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FDA 510(k)

ELASTIC GAUZE

K-Number: K802992 · 1980-12-30

Decision Date1980-12-30
Product CodeFQM
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

ELASTIC 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 1980-12-30 under 510(k) number K802992. The device is classified under product code FQM. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ELASTIC GAUZE?

ELASTIC GAUZE is a medical device that received FDA 510(k) clearance on 1980-12-30. The listed applicant is Abco Dealers, Inc.. The 510(k) number is K802992.

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

ELASTIC GAUZE received FDA 510(k) clearance on 1980-12-30, under 510(k) number K802992.

Who is the listed applicant for ELASTIC 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 ELASTIC GAUZE?

The FDA product code for ELASTIC GAUZE is FQM.

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 Abco Dealers, Inc. 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.

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Related Devices (Code: FQM)

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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