Stimulation Technology, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Stimulation Technology, Inc. - FDA 510(k) Cleared Devices
6
Total
6
Cleared
0
Denied
Stimulation Technology, Inc. has 6 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 6 cleared submissions from 1977 to 1979. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Stimulation Technology, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Stimulation Technology, Inc.
6 devices
Cleared
Jul 03, 1979
STIMTECH NEUROMUSCULAR STIMULATOR, C 600
Physical Medicine
27d
Cleared
Mar 21, 1979
STIMTECH TENS ELECTRODE
Neurology
28d
Cleared
Oct 11, 1978
ELECTRICAL NERVE STIMULATOR MODEL 6035
Neurology
28d
Cleared
Dec 15, 1977
NERVE STIMULATOR, ELEC. TRANSCUTANEOUS
Neurology
10d
Cleared
Mar 15, 1977
EPC INSTICKS
Neurology
7d
Cleared
Mar 15, 1977
INS - T.E.N.S.
Neurology
7d