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FDA 510(k), K970660, DERMAGRAN WOUND MANAGEMENT SYSTEM
FDA 510(k), K970660, DERMAGRAN WOUND MANAGEMENT SYSTEM
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510(K) Number: K970660
Device Name: DERMAGRAN WOUND MANAGEMENT SYSTEM
Manufacturer: DERMA SCIENCES, INC.
Device Classification Name: bandage, liquid
Regulation Number: 880.5090
Classification Product Code: KMF
Date Received: 02/21/1997
Decision Date: 08/12/1997
Regulation Medical Specialty: General Hospital
Device Name: DERMAGRAN WOUND MANAGEMENT SYSTEM
Manufacturer: DERMA SCIENCES, INC.
Device Classification Name: bandage, liquid
Regulation Number: 880.5090
Classification Product Code: KMF
Date Received: 02/21/1997
Decision Date: 08/12/1997
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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