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FDA 510(k), K142377, The OnControl Bone Marrow Biopsy System by Vidacare
FDA 510(k), K142377, The OnControl Bone Marrow Biopsy System by Vidacare
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510(K) Number: K142377
Device Name: The OnControl Bone Marrow Biopsy System by Vidacare
Manufacturer: VIDACARE LLC
Device Classification Name: instrument, biopsy
Regulation Number: 876.1075
Classification Product Code: KNW
Date Received: 08/26/2014
Decision Date: 12/17/2014
Regulation Medical Specialty: Gastroenterology/Urology
Device Name: The OnControl Bone Marrow Biopsy System by Vidacare
Manufacturer: VIDACARE LLC
Device Classification Name: instrument, biopsy
Regulation Number: 876.1075
Classification Product Code: KNW
Date Received: 08/26/2014
Decision Date: 12/17/2014
Regulation Medical Specialty: Gastroenterology/Urology
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks
NOTE: This document is not currently in our library. Upon purchase, we will request the document from the FDA FOIA office. Learn more about Fast-Track Requests here.
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