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
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
- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks
NOTE: This document is not currently in our library. Upon purchase, we will request the document from the FDA FOIA office. Learn more about Fast-Track Requests here.
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