Th Charters, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Th Charters, Inc. - FDA 510(k) Cleared Devices
8
Total
8
Cleared
0
Denied
Th Charters, Inc. has 8 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 8 cleared submissions from 1980 to 1987. Primary specialty: Physical Medicine.
Browse the FDA 510(k) cleared devices submitted by Th Charters, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Th Charters, Inc.
8 devices
Cleared
Oct 26, 1987
ELECTROBLOC TRANS. ELECTRICAL NERVE BLOCK GENERA.
Neurology
67d
Cleared
May 08, 1986
EXER-STIM 2
Neurology
15d
Cleared
Jul 19, 1985
REMOTE SPEED CONTROL
Physical Medicine
77d
Cleared
Jul 19, 1985
TORQUE FEEDBACK METER
Physical Medicine
74d
Cleared
Jan 03, 1984
MINI-1 TRANSCUTANEOUS ELEC-NERVE STIM
Neurology
29d
Cleared
Jul 19, 1983
NEURO-PULSER 2 TRANSCUTAN. ELEC. NERVE
Neurology
40d
Cleared
Oct 06, 1982
EXER-STIM CONTROLLER
Physical Medicine
85d
Cleared
Mar 19, 1980
STIM-EX 201
Physical Medicine
15d