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FDA 510(k), K083113, ACTICOAT FLEX 7 DRESSING
FDA 510(k), K083113, ACTICOAT FLEX 7 DRESSING
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510(K) Number: K083113
Device Name: ACTICOAT FLEX 7 DRESSING
Manufacturer: SMITH & NEPHEW, INC.
Device Classification Name: dressing, wound, drug
Regulation Number:
Classification Product Code: FRO
Date Received: 10/21/2008
Decision Date: 07/22/2009
Regulation Medical Specialty:
Device Name: ACTICOAT FLEX 7 DRESSING
Manufacturer: SMITH & NEPHEW, INC.
Device Classification Name: dressing, wound, drug
Regulation Number:
Classification Product Code: FRO
Date Received: 10/21/2008
Decision Date: 07/22/2009
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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