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FDA 510(k)

AUTOVAC CLOSED WOUND SUCTION SYSTEM

K-Number: K930615 · 1994-02-22

Decision Date1994-02-22
Product CodeGCY
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

AUTOVAC CLOSED WOUND SUCTION 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 1994-02-22 under 510(k) number K930615. The device is classified under product code GCY. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AUTOVAC CLOSED WOUND SUCTION SYSTEM?

AUTOVAC CLOSED WOUND SUCTION SYSTEM is a medical device that received FDA 510(k) clearance on 1994-02-22. The listed applicant is Boehringer Laboratories. The 510(k) number is K930615.

When did AUTOVAC CLOSED WOUND SUCTION SYSTEM receive FDA 510(k) clearance?

AUTOVAC CLOSED WOUND SUCTION SYSTEM received FDA 510(k) clearance on 1994-02-22, under 510(k) number K930615.

Who is the listed applicant for AUTOVAC CLOSED WOUND SUCTION 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 CLOSED WOUND SUCTION SYSTEM?

The FDA product code for AUTOVAC CLOSED WOUND SUCTION SYSTEM is GCY.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Other records listing Boehringer Laboratories as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

View all 38 devices →

Related Devices (Code: GCY)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Official Source

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

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