Omikron Scientific, Ltd. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Omikron Scientific, Ltd. - FDA 510(k) Cleared Devices
4
Total
3
Cleared
0
Denied
Omikron Scientific, Ltd. has 3 FDA 510(k) cleared medical devices. Based in Walker, US.
Historical record: 3 cleared submissions from 1984 to 1991. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Omikron Scientific, Ltd. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Omikron Scientific, Ltd.
4 devices
Cleared
Mar 06, 1991
OMIBAND
General & Plastic Surgery
159d
Cleared
Feb 22, 1988
MODIFIED MANUFACTURING PROCESS FOR OMIDERM(TM)
General & Plastic Surgery
112d
Cleared
Feb 15, 1985
OMIKRON PACEMAKER 837 UNIPOLAR & 838 BIPOLAR
Cardiovascular
102d
Cleared
Aug 03, 1984
LITHIUM PACEMAKER 811-811L & 811XL
Cardiovascular
162d