FDA 510(k), K050310, BARDPORT TITANIUM PORTS

FDA 510(k), K050310, BARDPORT TITANIUM PORTS

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510(K) Number: K050310
Device Name: BARDPORT TITANIUM PORTS
Manufacturer: BARD ACCESS SYSTEMS, INC.
Device Classification Name: port & catheter, implanted, subcutaneous, intravascular
Regulation Number: 880.5965
Classification Product Code: LJT
Date Received: 02/08/2005
Decision Date: 04/18/2005
Regulation Medical Specialty: General Hospital

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