FDA 510(k), K891696, DUODERM* EXTRA THIN FLEXIBLE HYDROCOLLOID DRESSING

FDA 510(k), K891696, DUODERM* EXTRA THIN FLEXIBLE HYDROCOLLOID DRESSING

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510(K) Number: K891696
Device Name: DUODERM* EXTRA THIN FLEXIBLE HYDROCOLLOID DRESSING
Manufacturer: CONVATEC, A DIVISION OF E.R. SQUIBB & SONS
Device Classification Name: dressing, wound, drug
Regulation Number:
Classification Product Code: FRO
Date Received: 03/22/1989
Decision Date: 05/04/1989

Total pages: 42
Fully redacted pages: 5
Content pages: 37

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