Omron Tateisi Electronics Co. - FDA 510(k) Cleared Devices
7
Total
7
Cleared
0
Denied
Omron Tateisi Electronics Co. has 7 FDA 510(k) cleared medical devices. Based in Tokyo, 105 Japan, JP.
Historical record: 7 cleared submissions from 1985 to 1988. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Omron Tateisi Electronics Co. Filter by specialty or product code using the sidebar.
7 devices
Cleared
Jun 15, 1988
OMRON DIGITAL BLOOD PRESSURE MONITOR MODEL HEM403C
Cardiovascular
63d
Cleared
Jun 15, 1988
OMRON DIGITAL BLOOD PRESSURE MONITOR MODEL HEM703C
Cardiovascular
63d
Cleared
Jun 12, 1987
DIGITAL SPHYGMOMANOMETER
Cardiovascular
66d
Cleared
Mar 26, 1987
OMRON ULTRASONIC NEBULIZER MODEL NE-UO5
Anesthesiology
134d
Cleared
Apr 17, 1986
OMRON DIGITAL BP MONITOR HEM-700CP
Cardiovascular
184d
Cleared
Nov 18, 1985
OMRON DIGITAL BP MONITOR HEM-700C
Cardiovascular
108d
Cleared
Jul 31, 1985
OMRON DIGITAL BP MONITOR HEM-400C
Cardiovascular
97d