Slenderizers Equipment Mfg., Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Slenderizers Equipment Mfg., Inc. - FDA 510(k) Cleared Devices
7
Total
7
Cleared
0
Denied
Slenderizers Equipment Mfg., Inc. has 7 FDA 510(k) cleared medical devices. Based in Arnold, US.
Historical record: 7 cleared submissions from 1987 to 1988. Primary specialty: Physical Medicine.
Browse the FDA 510(k) cleared devices submitted by Slenderizers Equipment Mfg., Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Slenderizers Equipment Mfg., Inc.
7 devices
Cleared
Jul 15, 1988
MULTI-FLEX TABLE--MODEL 200
Physical Medicine
78d
Cleared
Jun 09, 1987
MULTI-FLEX TABLE -- MODEL 101
Physical Medicine
109d
Cleared
Jun 09, 1987
MULTI-FLEX TABLE -- MODEL 102
Physical Medicine
109d
Cleared
Jun 09, 1987
MULTI-FLEX TABLE -- MODEL 103
Physical Medicine
109d
Cleared
Jun 09, 1987
MULTI-FLEX TABLE -- MODEL 104
Physical Medicine
109d
Cleared
Jun 09, 1987
MULTI-FLEX TABLE -- MODEL 105
Physical Medicine
109d
Cleared
Jun 09, 1987
MULTI-FLEX TABLE -- MODEL 106
Physical Medicine
109d