ACELL POWDER WOUND DRESSING
K-Number: K060888 · 2006-06-23
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Device Summary
Frequently Asked Questions
What is the ACELL POWDER WOUND DRESSING?
ACELL POWDER WOUND DRESSING is a medical device that received FDA 510(k) clearance on 2006-06-23. The listed applicant is Acell, Inc.. The 510(k) number is K060888.
When did ACELL POWDER WOUND DRESSING receive FDA 510(k) clearance?
ACELL POWDER WOUND DRESSING received FDA 510(k) clearance on 2006-06-23, under 510(k) number K060888.
Who is the listed applicant for ACELL POWDER WOUND DRESSING?
The FDA 510(k) record lists Acell, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ACELL POWDER WOUND DRESSING?
The FDA product code for ACELL POWDER 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.
Other records listing Acell, 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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