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FDA 510(k) K973716, DUODERM EXTRA THIN CGF DRESSING, by Convatec, A Bristol-Myers Squibb Co.

FDA 510(k) K973716, DUODERM EXTRA THIN CGF DRESSING, by Convatec, A Bristol-Myers Squibb Co.

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510(K) Number: K973716
Device Name: DUODERM EXTRA THIN CGF DRESSING
Manufacturer: Convatec, A Bristol-Myers Squibb Co.
Device Classification Name: dressing, wound and burn, occlusive
Regulation Number:
Classification Product Code: MGP
Date Received: 09/29/1997
Decision Date: 12/17/1997

Total pages: 179
Fully redacted pages: 6
Content pages: 173
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