J-Tech, Inc. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
J-Tech, Inc. has 5 FDA 510(k) cleared medical devices. Based in Midvale, US.
Historical record: 5 cleared submissions from 1991 to 1996. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by J-Tech, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by J-Tech, Inc.
5 devices
Cleared
Jul 03, 1996
SURFACE ELECTROMYOGRAPH BIOFEEDBACK MUSCLE ACTIVITY DEVICE
Neurology
261d
Cleared
Oct 30, 1995
INCLINOMETER
Neurology
20d
Cleared
May 10, 1995
LARGE MUSCLE STRENGTH GAUGE
Neurology
175d
Cleared
Oct 23, 1991
JTECH 50 SERIES CUTTING LOOP
Gastroenterology & Urology
72d
Cleared
Sep 05, 1991
GS-220 HAND IMPAIRMENT EVALUATION SYSTEM
Neurology
90d