COLLAWOUND DRESSING
K-Number: K061474 · 2006-07-05
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Device Summary
Frequently Asked Questions
What is the COLLAWOUND DRESSING?
COLLAWOUND DRESSING is a medical device that received FDA 510(k) clearance on 2006-07-05. The listed applicant is Collamatrix Co., Inc.. The 510(k) number is K061474.
When did COLLAWOUND DRESSING receive FDA 510(k) clearance?
COLLAWOUND DRESSING received FDA 510(k) clearance on 2006-07-05, under 510(k) number K061474.
Who is the listed applicant for COLLAWOUND DRESSING?
The FDA 510(k) record lists Collamatrix Co., Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for COLLAWOUND DRESSING?
The FDA product code for COLLAWOUND 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.
Other records listing Collamatrix Co., 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: 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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