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FDA 510(k) Applications Submitted by Mizuho America, Inc.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K955012
11/01/1995
MIZUHO RADIOLUCENT HEAD FRAME
MIZUHO AMERICA, INC.
K960037
01/03/1996
SUGITA AVM MICROCLIP
MIZUHO AMERICA, INC.
K211183
04/20/2021
Sugita AVM Microclips
Mizuho America, Inc.
K221524
05/26/2022
Sugita AVM Microclip Applier
Mizuho America, Inc.
K990202
01/21/1999
SUGITA TITANIUM ANEURYSM CLIP
MIZUHO AMERICA, INC.
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