FDA 510(k), K113872, THE ONCONTROL BONE ACCESS AND BONE BIOPSY SYSTEM BY VIDACARE

FDA 510(k), K113872, THE ONCONTROL BONE ACCESS AND BONE BIOPSY SYSTEM BY VIDACARE

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510(K) Number: K113872
Device Name: THE ONCONTROL BONE ACCESS AND BONE BIOPSY SYSTEM BY VIDACARE
Manufacturer:
Device Classification Name: Instrument, Biopsy
Regulation Number: 876.1075
Classification Product Code: KNW
Date Received: 12/30/2011
Decision Date: 03/08/2012
Regulation Medical Specialty: Gastroenterology/Urology
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