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FDA 510(k)

AUTOVAC CLOSED WOUND AUTOTRANSFUSION SYSTEM,7920 S

K-Number: K932093 · 1994-07-06

ApplicantBoehringer Laboratories
Decision Date1994-07-06
Product CodeCAC
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

AUTOVAC CLOSED WOUND AUTOTRANSFUSION SYSTEM,7920 S is the device name listed in this FDA 510(k) record. The listed applicant is Boehringer Laboratories. It received FDA 510(k) clearance on 1994-07-06 under 510(k) number K932093. 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 AUTOVAC CLOSED WOUND AUTOTRANSFUSION SYSTEM,7920 S?

AUTOVAC CLOSED WOUND AUTOTRANSFUSION SYSTEM,7920 S is a medical device that received FDA 510(k) clearance on 1994-07-06. The listed applicant is Boehringer Laboratories. The 510(k) number is K932093.

When did AUTOVAC CLOSED WOUND AUTOTRANSFUSION SYSTEM,7920 S receive FDA 510(k) clearance?

AUTOVAC CLOSED WOUND AUTOTRANSFUSION SYSTEM,7920 S received FDA 510(k) clearance on 1994-07-06, under 510(k) number K932093.

Who is the listed applicant for AUTOVAC CLOSED WOUND AUTOTRANSFUSION SYSTEM,7920 S?

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

What is the FDA product code for AUTOVAC CLOSED WOUND AUTOTRANSFUSION SYSTEM,7920 S?

The FDA product code for AUTOVAC CLOSED WOUND AUTOTRANSFUSION SYSTEM,7920 S 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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