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FDA 510(k)

ANERIOD GAUZE

K-Number: K812932 · 1981-12-02

ApplicantAbco Dealers, Inc.
Decision Date1981-12-02
Product CodeDXG
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

ANERIOD GAUZE is the device name listed in this FDA 510(k) record. The listed applicant is Abco Dealers, Inc.. It received FDA 510(k) clearance on 1981-12-02 under 510(k) number K812932. The device is classified under product code DXG. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ANERIOD GAUZE?

ANERIOD GAUZE is a medical device that received FDA 510(k) clearance on 1981-12-02. The listed applicant is Abco Dealers, Inc.. The 510(k) number is K812932.

When did ANERIOD GAUZE receive FDA 510(k) clearance?

ANERIOD GAUZE received FDA 510(k) clearance on 1981-12-02, under 510(k) number K812932.

Who is the listed applicant for ANERIOD GAUZE?

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

What is the FDA product code for ANERIOD GAUZE?

The FDA product code for ANERIOD GAUZE is DXG.

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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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