Mizuho USA, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Mizuho USA, Inc. - FDA 510(k) Cleared Devices
7
Total
7
Cleared
0
Denied
Mizuho USA, Inc. has 7 FDA 510(k) cleared medical devices. Based in San Diego, US.
Historical record: 7 cleared submissions from 1993 to 2006. Primary specialty: Chemistry.
Browse the FDA 510(k) cleared devices submitted by Mizuho USA, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Mizuho USA, Inc.
7 devices
Cleared
Jun 19, 2006
MULTI-USE ELECTRONIC PREGNANCY TEST
Chemistry
84d
Cleared
Apr 25, 2005
PROOF POSITIVE ELECTRONIC PREGNANCY TEST
Chemistry
154d
Cleared
Jun 16, 2000
ABSOLUTE HCG PREGNANCY TEST
Chemistry
93d
Cleared
Nov 07, 1996
NATURALE HCG PREGNANCY TES
Chemistry
31d
Cleared
Feb 10, 1995
QUICK CHECKER HCG PREGNANCY TEST
Chemistry
186d
Cleared
Jan 17, 1995
HCG MIDSTREAM PREGNANCY TEST
Chemistry
68d
Cleared
Sep 10, 1993
HCG MIDSTREAM PREGNANCY TEST
Chemistry
140d