Atlas FDA

PLEUR-EVAC AUTOTRANSFUSION SYSTEM -TENTATIVE

FDA 510(k) clearance K851024 · decided 1985-05-23

Clearance details

K-number
K851024
Device name
PLEUR-EVAC AUTOTRANSFUSION SYSTEM -TENTATIVE
Applicant
Pfizer, Inc.
Decision
Substantially Equivalent
Date received
1985-03-12
Decision date
1985-05-23
Days to decision
72 days
Clearance type
Traditional
Product code
CAC
Device class
2
Regulation number
868.5830
Medical specialty
Anesthesiology
Advisory committee
Anesthesiology
Location
Ny, NY, US
Third-party review
No
Expedited review
No

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Recalls involving this device

No recalls on record reference this clearance.

PMA approvals by this applicant

RecordFirmDate
GELFOAM (absorbable gelatin gel, powder from abs. gel, sponge USP), GELFOAM (compressed absorbable gelatin sponge, USP), (N18286/S041)Pfizer, Inc.2023-05-16
(Gelfoam (absorbable gelatin) Sterile Sponge) (N18286/S040)Pfizer, Inc.2022-06-24
Gelfoam (absorbable gelatin) Sterile Sponge (N18286/S039)Pfizer, Inc.2021-07-08
Gelfoam (absorbable gelatin) Sterile Sponge (N18286/S038)Pfizer, Inc.2021-05-07
Gelfoam Sterile Sponge (N18286/S037)Pfizer, Inc.2021-02-24
Gelfoam (absorbable gelatin) Sterile Sponge (N18286/S036)Pfizer, Inc.2020-12-10
Gelfoam (absorbable gelatin) Sterile Sponge (N18286/S035)Pfizer, Inc.2020-03-19
Gelfoam (absorbable gelatin) Sterile Sponge (N18286/S034)Pfizer, Inc.2020-02-27