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FDA 510(k), K143001, SILVERLON ISLAND WOUND DRESSING, SILVERLON WOUND PAD DRESSING
FDA 510(k), K143001, SILVERLON ISLAND WOUND DRESSING, SILVERLON WOUND PAD DRESSING
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510(K) Number: K143001
Device Name: SILVERLON ISLAND WOUND DRESSING, SILVERLON WOUND PAD DRESSING
Manufacturer: ARGENTUM MEDICAL
Device Classification Name: dressing, wound, drug
Regulation Number:
Classification Product Code: FRO
Date Received: 10/17/2014
Decision Date: 11/07/2014
Regulation Medical Specialty:
Device Name: SILVERLON ISLAND WOUND DRESSING, SILVERLON WOUND PAD DRESSING
Manufacturer: ARGENTUM MEDICAL
Device Classification Name: dressing, wound, drug
Regulation Number:
Classification Product Code: FRO
Date Received: 10/17/2014
Decision Date: 11/07/2014
Regulation Medical Specialty:
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