FDA 510(k), K973716, DUODERM EXTRA THIN CGF DRESSING

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