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FDA 510(k)

AUTOVAC(R) AUTOTRANSFUSION SYSTEM, 7900 SERIES

K-Number: K901138 · 1990-06-18

ApplicantBoehringer Laboratories
Decision Date1990-06-18
Product CodeCAC
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

AUTOVAC(R) AUTOTRANSFUSION SYSTEM, 7900 SERIES is the device name listed in this FDA 510(k) record. The listed applicant is Boehringer Laboratories. It received FDA 510(k) clearance on 1990-06-18 under 510(k) number K901138. 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(R) AUTOTRANSFUSION SYSTEM, 7900 SERIES?

AUTOVAC(R) AUTOTRANSFUSION SYSTEM, 7900 SERIES is a medical device that received FDA 510(k) clearance on 1990-06-18. The listed applicant is Boehringer Laboratories. The 510(k) number is K901138.

When did AUTOVAC(R) AUTOTRANSFUSION SYSTEM, 7900 SERIES receive FDA 510(k) clearance?

AUTOVAC(R) AUTOTRANSFUSION SYSTEM, 7900 SERIES received FDA 510(k) clearance on 1990-06-18, under 510(k) number K901138.

Who is the listed applicant for AUTOVAC(R) AUTOTRANSFUSION SYSTEM, 7900 SERIES?

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(R) AUTOTRANSFUSION SYSTEM, 7900 SERIES?

The FDA product code for AUTOVAC(R) AUTOTRANSFUSION SYSTEM, 7900 SERIES 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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