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FDA 510(k), K080949, KERATEC WOUND DRESSINGS
FDA 510(k), K080949, KERATEC WOUND DRESSINGS
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510(K) Number: K080949
Device Name: KERATEC WOUND DRESSINGS
Manufacturer: KERATEC LIMITED
Device Classification Name: dressing, wound, drug
Regulation Number:
Classification Product Code: FRO
Date Received: 04/03/2008
Decision Date: 02/11/2009
Regulation Medical Specialty:
Device Name: KERATEC WOUND DRESSINGS
Manufacturer: KERATEC LIMITED
Device Classification Name: dressing, wound, drug
Regulation Number:
Classification Product Code: FRO
Date Received: 04/03/2008
Decision Date: 02/11/2009
Regulation Medical Specialty:
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks when the FOIA office is operating at regular capacity
NOTE: This document is not currently in our library. Upon purchase, we will request the document from the FDA FOIA office. IMPORTANT: The FDA FOIA office operations are currently suspended. We are happy to make the request but do not know when we will receive a response. Learn more about Fast-Track Requests here.
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