Omron Electronics, Inc. - FDA 510(k) Cleared Devices
10
Total
10
Cleared
0
Denied
FDA 510(k) Regulatory Record - Omron Electronics, Inc. Cardiovascular ✕
4 devices
Cleared
Mar 06, 1990
OMRON DIGITAL BLOOD PRESSURE MONITOR MODEL HEM814F
Cardiovascular
228d
Cleared
Aug 30, 1988
DIGITAL BLOOD PRESSURE MONITOR MODEL HEM-703CP
Cardiovascular
81d
Cleared
Jun 16, 1988
OMRON DIGITAL BLOOD PRESSURE MONITOR HEM-701C
Cardiovascular
84d
Cleared
May 28, 1987
OMRON DIGITAL BLOOD PRESSURE MONITOR HEM-401C
Cardiovascular
64d