FDA 510(k), K914746, DERMAGRAN WET DRESSING

FDA 510(k), K914746, DERMAGRAN WET DRESSING

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510(K) Number: K914746
Device Name: DERMAGRAN WET DRESSING
Manufacturer: DERMA SCIENCES, INC.
Device Classification Name: dressing, wound and burn, hydrogel w/drug and/or biologic
Regulation Number:
Classification Product Code: MGQ
Date Received: 10/22/1991
Decision Date: 06/17/1992
Regulation Medical Specialty:

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