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FDA 510(k), K063202, PRODERMA LIQUID BANDAGE
FDA 510(k), K063202, PRODERMA LIQUID BANDAGE
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510(K) Number: K063202
Device Name: PRODERMA LIQUID BANDAGE
Manufacturer: PROCUREMENT TECHNOLOGY SYSTEMS, LLC
Device Classification Name: bandage, liquid
Regulation Number: 880.5090
Classification Product Code: KMF
Date Received: 10/20/2006
Decision Date: 05/02/2007
Regulation Medical Specialty: General Hospital
Device Name: PRODERMA LIQUID BANDAGE
Manufacturer: PROCUREMENT TECHNOLOGY SYSTEMS, LLC
Device Classification Name: bandage, liquid
Regulation Number: 880.5090
Classification Product Code: KMF
Date Received: 10/20/2006
Decision Date: 05/02/2007
Regulation Medical Specialty: General Hospital
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks
NOTE: This document is not currently in our library. Upon purchase, we will request the document from the FDA FOIA office. Learn more about Fast-Track Requests here.
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