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FDA 510(k)

AUTOVAC ORTHOPEDIC AUTOTRANSFUSION SYSTEM

K-Number: K014187 · 2002-02-06

ApplicantBoehringer Laboratories
Decision Date2002-02-06
Product CodeCAC
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

AUTOVAC ORTHOPEDIC AUTOTRANSFUSION SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Boehringer Laboratories. It received FDA 510(k) clearance on 2002-02-06 under 510(k) number K014187. 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 ORTHOPEDIC AUTOTRANSFUSION SYSTEM?

AUTOVAC ORTHOPEDIC AUTOTRANSFUSION SYSTEM is a medical device that received FDA 510(k) clearance on 2002-02-06. The listed applicant is Boehringer Laboratories. The 510(k) number is K014187.

When did AUTOVAC ORTHOPEDIC AUTOTRANSFUSION SYSTEM receive FDA 510(k) clearance?

AUTOVAC ORTHOPEDIC AUTOTRANSFUSION SYSTEM received FDA 510(k) clearance on 2002-02-06, under 510(k) number K014187.

Who is the listed applicant for AUTOVAC ORTHOPEDIC AUTOTRANSFUSION SYSTEM?

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 ORTHOPEDIC AUTOTRANSFUSION SYSTEM?

The FDA product code for AUTOVAC ORTHOPEDIC AUTOTRANSFUSION SYSTEM 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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