BIOBRANE BRAND TEMPORARY WOUND-DRESSING
K-Number: K801635 · 1980-08-04
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Device Summary
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 1980-08-04. The listed applicant is Hall-Woodroof, Inc.. The 510(k) number is K801635.
When did BIOBRANE BRAND TEMPORARY WOUND-DRESSING receive FDA 510(k) clearance?
BIOBRANE BRAND TEMPORARY WOUND-DRESSING received FDA 510(k) clearance on 1980-08-04, under 510(k) number K801635.
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.
What is the FDA product code for BIOBRANE BRAND TEMPORARY WOUND-DRESSING?
The FDA product code for BIOBRANE BRAND TEMPORARY WOUND-DRESSING is FRO. This falls under the Anesthesiology category.
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 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.
Related Devices (Code: FRO)
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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