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FDA 510(k)

ADHESIVE WOUND COVER FILM

K-Number: K822080 · 1982-10-15

Decision Date1982-10-15
Product CodeNAD
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

ADHESIVE WOUND COVER FILM is the device name listed in this FDA 510(k) record. The listed applicant is Hollister, Inc.. It received FDA 510(k) clearance on 1982-10-15 under 510(k) number K822080. The device is classified under product code NAD. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ADHESIVE WOUND COVER FILM?

ADHESIVE WOUND COVER FILM is a medical device that received FDA 510(k) clearance on 1982-10-15. The listed applicant is Hollister, Inc.. The 510(k) number is K822080.

When did ADHESIVE WOUND COVER FILM receive FDA 510(k) clearance?

ADHESIVE WOUND COVER FILM received FDA 510(k) clearance on 1982-10-15, under 510(k) number K822080.

Who is the listed applicant for ADHESIVE WOUND COVER FILM?

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

What is the FDA product code for ADHESIVE WOUND COVER FILM?

The FDA product code for ADHESIVE WOUND COVER FILM is NAD.

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 Hollister, 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: NAD)

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

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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