FDA 510(k), K100591, SORBACT
FDA 510(k), K100591, SORBACT
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510(K) Number: K100591
Device Name: SORBACT
Manufacturer: ABIGO MEDICAL AB
Device Classification Name: dressing, wound, drug
Regulation Number:
Classification Product Code: FRO
Date Received: 03/02/2010
Decision Date: 01/24/2011
Regulation Medical Specialty:
Device Name: SORBACT
Manufacturer: ABIGO MEDICAL AB
Device Classification Name: dressing, wound, drug
Regulation Number:
Classification Product Code: FRO
Date Received: 03/02/2010
Decision Date: 01/24/2011
Regulation Medical Specialty:
- 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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