FDA 510(k) Applications Submitted by MIZUHO USA, INC.

FDA 510(k) Number Submission Date Device Name Applicant
K000844 03/15/2000 ABSOLUTE HCG PREGNANCY TEST MIZUHO USA, INC.
K060825 03/27/2006 MULTI-USE ELECTRONIC PREGNANCY TEST MIZUHO USA, INC.
K964002 10/07/1996 NATURALE HCG PREGNANCY TES MIZUHO USA, INC.
K043231 11/22/2004 PROOF POSITIVE ELECTRONIC PREGNANCY TEST MIZUHO USA, INC.


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