Stereotactic Medical Systems, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Stereotactic Medical Systems, Inc. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Stereotactic Medical Systems, Inc. has 5 FDA 510(k) cleared medical devices. Based in New Harford, US.
Historical record: 5 cleared submissions from 1986 to 1989. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Stereotactic Medical Systems, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Stereotactic Medical Systems, Inc.
5 devices
Cleared
Dec 06, 1989
COMPASS(TM) STEREOTACTIC RETRACTOR SYSTEM
Neurology
43d
Cleared
Feb 28, 1989
EP-100 (SERIES)
Gastroenterology & Urology
131d
Cleared
Nov 01, 1988
EP-100 INFUSION PUMP
General Hospital
67d
Cleared
May 08, 1987
COMPASS STEREOTACTIC POSITIONING SYSTEM
Neurology
52d
Cleared
Jun 18, 1986
COMPASS CT STEREOTACTIC ADAPTATION SYSTEM
Neurology
7d