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FDA 510(k)

ROLL STRETCH GAUZE

K-Number: K802991 · 1980-12-30

ApplicantAbco Dealers, Inc.
Decision Date1980-12-30
Product CodeFQM
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

ROLL STRETCH 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 K802991. 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 ROLL STRETCH GAUZE?

ROLL STRETCH 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 K802991.

When did ROLL STRETCH GAUZE receive FDA 510(k) clearance?

ROLL STRETCH GAUZE received FDA 510(k) clearance on 1980-12-30, under 510(k) number K802991.

Who is the listed applicant for ROLL STRETCH 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 ROLL STRETCH GAUZE?

The FDA product code for ROLL STRETCH GAUZE is FQM.

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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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