Electro Therapeutic Devices, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Electro Therapeutic Devices, Inc. - FDA 510(k) Cleared Devices
8
Total
8
Cleared
0
Denied
Electro Therapeutic Devices, Inc. has 8 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 8 cleared submissions from 1977 to 1998. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Electro Therapeutic Devices, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Electro Therapeutic Devices, Inc.
8 devices
Cleared
Aug 24, 1998
ADDIQUIP DISPOSABLE ACUPUNCTURE NEEDLES
General Hospital
139d
Cleared
Sep 08, 1989
ELECTRICAL MUSCLE STIMULATOR MODEL MYOAID
Physical Medicine
619d
Cleared
Oct 24, 1986
'TENSAID'
Neurology
42d
Cleared
Oct 24, 1986
'MYOSTIM EX'
Neurology
42d
Cleared
Dec 04, 1985
TRANSCUTANEOUS ELECTR. NERVE STIMUL MYOSTIM 804
Neurology
90d
Cleared
Dec 04, 1985
TRANSCUTANEOUS ELECT. NERVE STIMUL-MYOSTIM 410
Neurology
90d
Cleared
Aug 17, 1984
ETI TENS BELT
Neurology
9d
Cleared
Jul 14, 1977
THERATHERM
Physical Medicine
93d