COLLAGEN WOUND DRESSING
K-Number: K002443 · 2000-10-18
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Device Summary
Frequently Asked Questions
What is the COLLAGEN WOUND DRESSING?
COLLAGEN WOUND DRESSING is a medical device that received FDA 510(k) clearance on 2000-10-18. The listed applicant is Oasis Research, LLC. The 510(k) number is K002443.
When did COLLAGEN WOUND DRESSING receive FDA 510(k) clearance?
COLLAGEN WOUND DRESSING received FDA 510(k) clearance on 2000-10-18, under 510(k) number K002443.
Who is the listed applicant for COLLAGEN WOUND DRESSING?
The FDA 510(k) record lists Oasis Research, LLC as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for COLLAGEN WOUND DRESSING?
The FDA product code for COLLAGEN WOUND DRESSING is KGN.
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.
Related Devices (Code: KGN)
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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