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FDA 510(k)

BIOBRANE BRAND TEMPORARY WOUND DRESSING

K-Number: K791184 · 1979-11-15

ApplicantHall-Woodroof, Inc.
Decision Date1979-11-15
Product Code
DecisionSubstantially Equivalent

Device Summary

BIOBRANE BRAND TEMPORARY WOUND DRESSING is the device name listed in this FDA 510(k) record. The listed applicant is Hall-Woodroof, Inc.. It received FDA 510(k) clearance on 1979-11-15 under 510(k) number K791184. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BIOBRANE BRAND TEMPORARY WOUND DRESSING?

BIOBRANE BRAND TEMPORARY WOUND DRESSING is a medical device that received FDA 510(k) clearance on 1979-11-15. The listed applicant is Hall-Woodroof, Inc.. The 510(k) number is K791184.

When did BIOBRANE BRAND TEMPORARY WOUND DRESSING receive FDA 510(k) clearance?

BIOBRANE BRAND TEMPORARY WOUND DRESSING received FDA 510(k) clearance on 1979-11-15, under 510(k) number K791184.

Who is the listed applicant for BIOBRANE BRAND TEMPORARY WOUND DRESSING?

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

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.

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Other records listing Hall-Woodroof, 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.

K801635BIOBRANE BRAND TEMPORARY WOUND-DRESSING

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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