FDA 510(k), K926139, CATHLINK 20 TITANIUM PORT W/ATT. POLYURETHANE CATH

FDA 510(k), K926139, CATHLINK 20 TITANIUM PORT W/ATT. POLYURETHANE CATH

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510(K) Number: K926139
Device Name: CATHLINK 20 TITANIUM PORT W/ATT. POLYURETHANE CATH
Manufacturer:
Device Classification Name: Port & Catheter, Implanted, Subcutaneous, Intravascular
Regulation Number: 880.5965
Classification Product Code: LJT
Date Received: 12/07/1992
Decision Date: 01/03/1995
Regulation Medical Specialty: General Hospital
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