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FDA 510(k), K925990, DUODERM EXTRA THIN CGF DRESSING
FDA 510(k), K925990, DUODERM EXTRA THIN CGF DRESSING
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510(K) Number: K925990
Device Name: DUODERM EXTRA THIN CGF DRESSING
Manufacturer: CONVATEC, A DIVISION OF E.R. SQUIBB & SONS
Device Classification Name: bandage, liquid
Regulation Number: 880.5090
Classification Product Code: KMF
Date Received: 11/25/1992
Decision Date: 10/28/1993
Regulation Medical Specialty: General Hospital
Device Name: DUODERM EXTRA THIN CGF DRESSING
Manufacturer: CONVATEC, A DIVISION OF E.R. SQUIBB & SONS
Device Classification Name: bandage, liquid
Regulation Number: 880.5090
Classification Product Code: KMF
Date Received: 11/25/1992
Decision Date: 10/28/1993
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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