FDA 510(k), K990202, SUGITA TITANIUM ANEURYSM CLIP

FDA 510(k), K990202, SUGITA TITANIUM ANEURYSM CLIP

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510(K) Number: K990202
Device Name: SUGITA TITANIUM ANEURYSM CLIP
Manufacturer: MIZUHO AMERICA, INC.
Device Classification Name: clip, aneurysm
Regulation Number: 882.5200
Classification Product Code: HCH
Date Received: 01/21/1999
Decision Date: 06/04/1999
Regulation Medical Specialty: Neurology

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