FDA 510(k), K983210, ALGISITE M
FDA 510(k), K983210, ALGISITE M
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510(K) Number: K983210
Device Name: ALGISITE M
Manufacturer:
Device Classification Name: Bandage, Liquid
Regulation Number: 880.5090
Classification Product Code: KMF
Date Received: 09/14/1998
Decision Date: 12/10/1998
Regulation Medical Specialty: General Hospital
Device Name: ALGISITE M
Manufacturer:
Device Classification Name: Bandage, Liquid
Regulation Number: 880.5090
Classification Product Code: KMF
Date Received: 09/14/1998
Decision Date: 12/10/1998
Regulation Medical Specialty: General Hospital