FDA 510(k), K970864, ARROW-HOWES LARGE BORE MULTI-LUMEN CENTRAL VENOUS CATHETERS

FDA 510(k), K970864, ARROW-HOWES LARGE BORE MULTI-LUMEN CENTRAL VENOUS CATHETERS

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510(K) Number: K970864
Device Name: ARROW-HOWES LARGE BORE MULTI-LUMEN CENTRAL VENOUS CATHETERS
Manufacturer:
Device Classification Name: Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days
Regulation Number: 880.5200
Classification Product Code: FOZ
Date Received: 03/10/1997
Decision Date: 10/17/1997
Regulation Medical Specialty: General Hospital
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