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FDA 510(k), K973716, DUODERM EXTRA THIN CGF DRESSING
FDA 510(k), K973716, DUODERM EXTRA THIN CGF DRESSING
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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
Regulation Medical Specialty:
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
Regulation Medical Specialty:
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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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