Prosecution Insights
Last updated: July 17, 2026
Application No. 18/757,672

SYSTEM AND METHOD FOR PROCESSING OF WHOLE BLOOD INTO PLASMA PRODUCTS OF DIFFERENT CATEGORIZATION

Non-Final OA §103
Filed
Jun 28, 2024
Priority
Jun 30, 2023 — provisional 63/511,377 +1 more
Examiner
DEAK, LESLIE R
Art Unit
3781
Tech Center
3700 — Mechanical Engineering & Manufacturing
Assignee
Fenwal Inc.
OA Round
1 (Non-Final)
75%
Grant Probability
Favorable
1-2
OA Rounds
1y 2m
Est. Remaining
93%
With Interview

Examiner Intelligence

Grants 75% — above average
75%
Career Allowance Rate
710 granted / 943 resolved
+5.3% vs TC avg
Strong +18% interview lift
Without
With
+17.6%
Interview Lift
resolved cases with interview
Typical timeline
3y 3m
Avg Prosecution
34 currently pending
Career history
982
Total Applications
across all art units

Statute-Specific Performance

§101
0.8%
-39.2% vs TC avg
§103
72.3%
+32.3% vs TC avg
§102
7.0%
-33.0% vs TC avg
§112
0.9%
-39.1% vs TC avg
Black line = Tech Center average estimate • Based on career data from 943 resolved cases

Office Action

§103
DETAILED ACTION Notice of Pre-AIA or AIA Status The present application, filed on or after March 16, 2013, is being examined under the first inventor to file provisions of the AIA . Claim Rejections - 35 USC § 103 The following is a quotation of 35 U.S.C. 103 which forms the basis for all obviousness rejections set forth in this Office action: A patent for a claimed invention may not be obtained, notwithstanding that the claimed invention is not identically disclosed as set forth in section 102, if the differences between the claimed invention and the prior art are such that the claimed invention as a whole would have been obvious before the effective filing date of the claimed invention to a person having ordinary skill in the art to which the claimed invention pertains. Patentability shall not be negated by the manner in which the invention was made. Claims 1-11 are rejected under 35 U.S.C. 103 as being unpatentable over US 8,075,468 to Min et al in view of Hardwick (as cited by Applicant). In the specification and figures, Min discloses the apparatus substantially as claimed by Applicant. With regard to claims 1, 6, Min discloses a reusable centrifuge, pump, and valve assembly for use with a disposable fluid flow circuit (see FIG 2 and accompanying text, col 1 ln 22-26). The disposable circuit comprises a processing chamber 18, a blood supply container 312, a plasma collection container 304, a red blood cell container 308 (see col 7, ln 51-55; col 12, ln 18-32). A controller may be used to run various blood collection applications 254, which may vary (see col 18, ln 13-23). In a red blood cell and plasma collection procedure, the pump and valve system convey whole blood to a separation system, separating WB into plasma and red blood cells, collecting each in their respective containers (see col 34, ln 15-51). Min further discloses collection of a third component, the buffy coat, in a third container 376 (see col 59, ln 39-67). Min also discloses that the apparatus may be programmed in many different ways, including process to retain some of the plasma for storage or fractionation purposes (see col 61, ln 63 to col 62, ln 9). Min does not expressly disclose the step of separating the plasma into two separate containers. However, Hardwick discloses that it is known in the art to process whole blood into various parts such that the components may be stored under ideal conditions, and maximizes the use of a single donation (see FIG 11-1, p 148). To that end, Hardwick illustrates a procedure wherein whole blood is separated into red cells, plasma, and platelets, wherein the plasma is further separated into a first portion of liquid plasma for therapeutic purposes, and a second portion for fractionation in order to maximize the use of excess plasma (see p163, 170-171). It would have been obvious to a person having ordinary skill in the art at the time of filing to program the Min apparatus to separate collected plasma into separate parts such as fresh plasma, and plasma for fractionation, in order to maximize a single donation, as taught by Hardwick. With regard to claims 2, 7 and 8, Min discloses that fluid weight may be used to determine target collection volumes and control the system (see col 19, ln 9-20). With regard to claims 3-4, 9-10, Min discloses that the system may be programmed to move the fluid in a manner consistent with the desired collection protocol (see col 98, ln 44-68). With regard to claims 5, 11, Min discloses the use of an additive solution being combined with collected red blood cells (see col 91, ln 42-col 92, ln 34). Allowable Subject Matter Claims 12-21 are objected to as being dependent upon a rejected base claim, but would be allowable if rewritten in independent form including all of the limitations of the base claim and any intervening claims. The following is a statement of reasons for the indication of allowable subject matter: While the prior art generally teaches an apparatus for separating and collecting two separate plasma products in an apheresis session, the prior art fails to teach the priming steps claimed by Applicant. While Min discloses a priming operation, Min does not teach an apparatus with a controller that is programmed to execute a priming stage in which a controller controls a centrifuge to rotate at a first and second target rate or first and second target orientation while pumping fluid, along with the other steps and limitations of the claims. Conclusion Any inquiry concerning this communication or earlier communications from the examiner should be directed to LESLIE R DEAK whose telephone number is (571)272-4943. The examiner can normally be reached Monday-Friday, 9am to 5:30pm. Examiner interviews are available via telephone, in-person, and video conferencing using a USPTO supplied web-based collaboration tool. To schedule an interview, applicant is encouraged to use the USPTO Automated Interview Request (AIR) at http://www.uspto.gov/interviewpractice. If attempts to reach the examiner by telephone are unsuccessful, the examiner’s supervisor, Sarah Al-Hashimi can be reached at 571-272-7159. The fax phone number for the organization where this application or proceeding is assigned is 571-273-8300. Information regarding the status of published or unpublished applications may be obtained from Patent Center. Unpublished application information in Patent Center is available to registered users. To file and manage patent submissions in Patent Center, visit: https://patentcenter.uspto.gov. Visit https://www.uspto.gov/patents/apply/patent-center for more information about Patent Center and https://www.uspto.gov/patents/docx for information about filing in DOCX format. For additional questions, contact the Electronic Business Center (EBC) at 866-217-9197 (toll-free). If you would like assistance from a USPTO Customer Service Representative, call 800-786-9199 (IN USA OR CANADA) or 571-272-1000. /LESLIE R DEAK/Primary Examiner, Art Unit 3799 10 June 2026
Read full office action

Prosecution Timeline

Jun 28, 2024
Application Filed
Jun 23, 2026
Non-Final Rejection mailed — §103 (current)

Precedent Cases

Applications granted by this same examiner with similar technology

Patent 12678550
NEW STANDARDIZATIONS & MEDICAL DEVICES FOR THE PREPARATION OF PLATELET RICH PLASMA (PRP) OR BONE MARROW CONCENTRATE (BMC) ALONE OR IN COMBINATION WITH HYALURONIC ACID
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INTRAOCULAR SHUNTS WITH LOW-PROFILE ACTUATION ELEMENTS AND ASSOCIATED SYSTEMS AND METHODS
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Patent 12667488
SHUNTING SYSTEMS WITH ROTATION-BASED FLOW CONTROL ASSEMBLIES, AND ASSOCIATED SYSTEMS AND METHODS
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Patent 12661264
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3y 3m to grant Granted Jun 23, 2026
Study what changed to get past this examiner. Based on 5 most recent grants.

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Prosecution Projections

1-2
Expected OA Rounds
75%
Grant Probability
93%
With Interview (+17.6%)
3y 3m (~1y 2m remaining)
Median Time to Grant
Low
PTA Risk
Based on 943 resolved cases by this examiner. Grant probability derived from career allowance rate.

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