Omron Electronics, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Omron Electronics, Inc. - FDA 510(k) Cleared Devices
10
Total
10
Cleared
0
Denied
Omron Electronics, Inc. has 10 FDA 510(k) cleared medical devices. Based in Schaumburg, US.
Historical record: 10 cleared submissions from 1987 to 1990. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Omron Electronics, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Omron Electronics, Inc.
10 devices
Cleared
Oct 31, 1990
OMRON PULSE STIMULATOR MODEL HV-F05
Physical Medicine
163d
Cleared
Mar 06, 1990
OMRON DIGITAL BLOOD PRESSURE MONITOR MODEL HEM814F
Cardiovascular
228d
Cleared
May 31, 1989
OMRON TRAVEL MASSAGER, MODEL HM-01
Physical Medicine
37d
Cleared
Oct 04, 1988
OMRON DIGITAL FEVER THERMOMETER MODEL MC-3
General Hospital
183d
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
Jul 23, 1987
OMRON DIGITAL FEVER THERMOMETER MODEL MC-12B
General Hospital
28d
Cleared
Jun 17, 1987
DIGITAL FEVER THERMOMETER MODEL MC-5
General Hospital
34d
Cleared
May 28, 1987
OMRON DIGITAL BLOOD PRESSURE MONITOR HEM-401C
Cardiovascular
64d
Cleared
Apr 16, 1987
OMRON DIGITAL FEVER THERMOMETER MODEL MC-7
General Hospital
37d