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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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- Delivery: Approximately 1 to 2 weeks when the FOIA office is operating at regular capacity
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