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.


Search | Companies | Product Codes | Device Names | Contacts | Applications | Decisions | Contact