FDA 510(k) K924250, PLASTIC LOW PROFILE SUBCUTANEOUS PORT, BARD ACCESS SYSTEMS, INC.
FDA 510(k) K924250, PLASTIC LOW PROFILE SUBCUTANEOUS PORT, BARD ACCESS SYSTEMS, INC.
Device Name: PLASTIC LOW PROFILE SUBCUTANEOUS PORT
Manufacturer: BARD ACCESS SYSTEMS, INC.
Device Classification Name: Port & Catheter, Implanted, Subcutaneous, Intravascular
Regulation Number: 880.5965
Classification Product Code: LJT
Date Received: 08/24/1992
Decision Date: 10/04/1993
Regulation Medical Specialty: General Hospital
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