Theratech, Inc.

FDA Regulatory Profile

Summary

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

Recent 510(k) Clearances

K-NumberDeviceDate
K060975IF TRUE SINE INTERFERENTIAL STIMULATOR / MODEL WL-2206A1 & WI-2206A2May 10, 2006
K050847IF TRUE SINE INTERFERENTIAL STIMULATOR, MODEL WL-2206AJune 17, 2005
K024100IF SERIES TRUE SINE INTERFERENTIAL STIMULATOR/MODEL: WL-2206, WELL IF, LIFE IF AND THE CUSTOMER PRIVFebruary 25, 2003
K021436TTECH MODEL 200E + TENS DEVICEJuly 30, 2002
K013768POWERED MUSCLE STIMULATORJuly 3, 2002