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:

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