FDA 510(k), K071202, DERMAPORT PERCUTANEOUS VASCULAR ACCESS SYSTEM (PVAS)

FDA 510(k), K071202, DERMAPORT PERCUTANEOUS VASCULAR ACCESS SYSTEM (PVAS)

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510(K) Number: K071202
Device Name: DERMAPORT PERCUTANEOUS VASCULAR ACCESS SYSTEM (PVAS)
Manufacturer:
Device Classification Name: Catheter, Hemodialysis, Implanted
Regulation Number: 876.5540
Classification Product Code: MSD
Date Received: 05/01/2007
Decision Date: 11/30/2007
Regulation Medical Specialty: Gastroenterology/Urology
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