Oms Medico, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Oms Medico, Inc. - FDA 510(k) Cleared Devices
7
Total
7
Cleared
0
Denied
Oms Medico, Inc. has 7 FDA 510(k) cleared medical devices. Based in Braintree, US.
Historical record: 7 cleared submissions from 1987 to 1987. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Oms Medico, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Oms Medico, Inc.
7 devices
Cleared
Nov 20, 1987
TX-2(TENS)
Neurology
29d
Cleared
Nov 20, 1987
TX-4(TENS) (SIGMA TENS)
Neurology
16d
Cleared
Oct 08, 1987
GLOBALCARE(TENS)
Neurology
43d
Cleared
Sep 16, 1987
120Z(TENS)
Neurology
16d
Cleared
Jun 25, 1987
TX-3(TENS)
Neurology
55d
Cleared
Mar 17, 1987
UNI-PULS(TENS) MODEL #292
Neurology
83d
Cleared
Mar 17, 1987
NEU-PULS(TENS) MODEL #295
Neurology
34d