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FDA 510(k), K961901, BONE & MARROW COLLECTION SYSTEM
FDA 510(k), K961901, BONE & MARROW COLLECTION SYSTEM
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510(K) Number: K961901
Device Name: BONE & MARROW COLLECTION SYSTEM
Manufacturer: BIOMEDICAL ENT., INC.
Device Classification Name: motor, surgical instrument, ac-powered
Regulation Number: 878.4820
Classification Product Code: GEY
Date Received: 05/16/1996
Decision Date: 08/06/1996
Regulation Medical Specialty: General & Plastic Surgery
Device Name: BONE & MARROW COLLECTION SYSTEM
Manufacturer: BIOMEDICAL ENT., INC.
Device Classification Name: motor, surgical instrument, ac-powered
Regulation Number: 878.4820
Classification Product Code: GEY
Date Received: 05/16/1996
Decision Date: 08/06/1996
Regulation Medical Specialty: General & Plastic Surgery
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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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