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FDA 510(k), K041995, MODIFICATION TO: GP GENERAL PURPOSE DRAINAGE CATHETER, MINI-PIG DRAINAGE CATHETER, NEPHROSTOMY CATHETER, BILIARY
FDA 510(k), K041995, MODIFICATION TO: GP GENERAL PURPOSE DRAINAGE CATHETER, MINI-PIG DRAINAGE CATHETER, NEPHROSTOMY CATHETER, BILIARY
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510(K) Number: K041995
Device Name: MODIFICATION TO: GP GENERAL PURPOSE DRAINAGE CATHETER, MINI-PIG DRAINAGE CATHETER, NEPHROSTOMY CATHETER, BILIARY
Manufacturer: URESIL, LLC
Device Classification Name: catheter, nephrostomy, general & plastic surgery
Regulation Number: 878.4200
Classification Product Code: GBO
Date Received: 07/23/2004
Decision Date: 08/19/2004
Regulation Medical Specialty: General & Plastic Surgery
Device Name: MODIFICATION TO: GP GENERAL PURPOSE DRAINAGE CATHETER, MINI-PIG DRAINAGE CATHETER, NEPHROSTOMY CATHETER, BILIARY
Manufacturer: URESIL, LLC
Device Classification Name: catheter, nephrostomy, general & plastic surgery
Regulation Number: 878.4200
Classification Product Code: GBO
Date Received: 07/23/2004
Decision Date: 08/19/2004
Regulation Medical Specialty: General & Plastic Surgery
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