J-Tech, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
5
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K954737SURFACE ELECTROMYOGRAPH BIOFEEDBACK MUSCLE ACTIVITY DEVICEJuly 3, 1996
K954647INCLINOMETEROctober 30, 1995
K945630LARGE MUSCLE STRENGTH GAUGEMay 10, 1995
K913587JTECH 50 SERIES CUTTING LOOPOctober 23, 1991
K912526GS-220 HAND IMPAIRMENT EVALUATION SYSTEMSeptember 5, 1991