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FDA 510(k), K002599, MODIFICATION TO ACRYDERM SILVER ANTIMICROBIAL WOUND DRESSING, MODELS 1041, 1042, 1043, 1044, 1045
FDA 510(k), K002599, MODIFICATION TO ACRYDERM SILVER ANTIMICROBIAL WOUND DRESSING, MODELS 1041, 1042, 1043, 1044, 1045
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510(K) Number: K002599
Device Name: MODIFICATION TO ACRYDERM SILVER ANTIMICROBIAL WOUND DRESSING, MODELS 1041, 1042, 1043, 1044, 1045
Manufacturer: BRUCE GIBBONS
Device Classification Name: Dressing, Wound, Drug
Regulation Number: FRO
Classification Product Code: 08/21/2000
Date Received: 09/21/2000
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: General & Plastic Surgery
Device Name: MODIFICATION TO ACRYDERM SILVER ANTIMICROBIAL WOUND DRESSING, MODELS 1041, 1042, 1043, 1044, 1045
Manufacturer: BRUCE GIBBONS
Device Classification Name: Dressing, Wound, Drug
Regulation Number: FRO
Classification Product Code: 08/21/2000
Date Received: 09/21/2000
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: General & Plastic Surgery
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks
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