S & W Enterprises, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
S & W Enterprises, Inc. - FDA 510(k) Cleared Devices
6
Total
6
Cleared
0
Denied
S & W Enterprises, Inc. has 6 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 6 cleared submissions from 1983 to 1987. Primary specialty: Physical Medicine.
Browse the FDA 510(k) cleared devices submitted by S & W Enterprises, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - S & W Enterprises, Inc.
6 devices
Cleared
Jan 05, 1987
S&W MODEL HIGH-LOW MAT TABLE, VARIOUS MODELS
Physical Medicine
27d
Cleared
Apr 13, 1984
TILT TABLE 53
Physical Medicine
28d
Cleared
Sep 20, 1983
S & W SW52E W/POWER BACK LIFT
General Hospital
35d
Cleared
May 13, 1983
S & W MODEL ASO
Obstetrics & Gynecology
56d
Cleared
Apr 08, 1983
S & W MODEL SW 37
Physical Medicine
21d
Cleared
Apr 08, 1983
S & W MODEL 29
Physical Medicine
21d