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FDA 510(k)

PLEUR-EVAC AUTOTRANSFUSION SYSTEM -TENTATIVE

K-Number: K851024 · 1985-05-23

ApplicantPfizer, Inc.
Decision Date1985-05-23
Product CodeCAC
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

PLEUR-EVAC AUTOTRANSFUSION SYSTEM -TENTATIVE is the device name listed in this FDA 510(k) record. The listed applicant is Pfizer, Inc.. It received FDA 510(k) clearance on 1985-05-23 under 510(k) number K851024. The device is classified under product code CAC. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PLEUR-EVAC AUTOTRANSFUSION SYSTEM -TENTATIVE?

PLEUR-EVAC AUTOTRANSFUSION SYSTEM -TENTATIVE is a medical device that received FDA 510(k) clearance on 1985-05-23. The listed applicant is Pfizer, Inc.. The 510(k) number is K851024.

When did PLEUR-EVAC AUTOTRANSFUSION SYSTEM -TENTATIVE receive FDA 510(k) clearance?

PLEUR-EVAC AUTOTRANSFUSION SYSTEM -TENTATIVE received FDA 510(k) clearance on 1985-05-23, under 510(k) number K851024.

Who is the listed applicant for PLEUR-EVAC AUTOTRANSFUSION SYSTEM -TENTATIVE?

The FDA 510(k) record lists Pfizer, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PLEUR-EVAC AUTOTRANSFUSION SYSTEM -TENTATIVE?

The FDA product code for PLEUR-EVAC AUTOTRANSFUSION SYSTEM -TENTATIVE is CAC.

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Related Devices (Code: CAC)

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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