Minnesota Scientific, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Minnesota Scientific, Inc. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Minnesota Scientific, Inc. has 5 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 5 cleared submissions from 1981 to 1987. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Minnesota Scientific, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Minnesota Scientific, Inc.
5 devices
Cleared
Aug 11, 1987
OMNI-TRACT CORRAL RETRACTOR
General & Plastic Surgery
15d
Cleared
Oct 16, 1985
OMNI-TRACT CHEST WALL & LUNA RETRACTOR
General & Plastic Surgery
22d
Cleared
Oct 16, 1985
MINNESOTA SCIENTIFIC, INC. OMNI-BEAM
General & Plastic Surgery
22d
Cleared
Aug 17, 1984
OMNI-TRACT SURGICAL RETRACTOR SYS
General & Plastic Surgery
32d
Cleared
Feb 26, 1981
OPERATING TABLE ACCESSORY CLAMP
General & Plastic Surgery
24d