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FDA 510(k), K960037, SUGITA AVM MICROCLIP
FDA 510(k), K960037, SUGITA AVM MICROCLIP
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510(K) Number: K960037
Device Name: SUGITA AVM MICROCLIP
Manufacturer: MIZUHO AMERICA, INC.
Device Classification Name: clip, aneurysm
Regulation Number: 882.5200
Classification Product Code: HCH
Date Received: 01/03/1996
Decision Date: 02/05/1997
Regulation Medical Specialty: Neurology
Device Name: SUGITA AVM MICROCLIP
Manufacturer: MIZUHO AMERICA, INC.
Device Classification Name: clip, aneurysm
Regulation Number: 882.5200
Classification Product Code: HCH
Date Received: 01/03/1996
Decision Date: 02/05/1997
Regulation Medical Specialty: Neurology
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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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