Medical Device Manufacturer · US , Great Neck , NY

Theratech, Inc. - FDA 510(k) Cleared Devices

5 submissions · 5 cleared · Since 2002

Recent clearances: IF TRUE SINE INTERFERENTIAL STIMULATOR / MODEL WL-2206A1 & WI-2206A2, IF TRUE SINE INTERFERENTIAL STIMULATOR, MODEL WL-2206A, IF SERIES TRUE SINE INTERFERENTIAL STIMULATOR/MODEL: WL-2206, WELL IF, LIFE IF AND THE CUSTOMER PRIVATE BRAND

View 5 510(k) Devices ↓

5

Total

5

Cleared

0

Denied

FDA 510(k) Regulatory Record - Theratech, Inc. Neurology ✕

3 devices

1-3 of 3

Cleared May 10, 2006

IF TRUE SINE INTERFERENTIAL STIMULATOR / MODEL WL-2206A1 & WI-2206A2

Neurology · 30d

Cleared Feb 25, 2003

IF SERIES TRUE SINE INTERFERENTIAL STIMULATOR/MODEL: WL-2206, WELL IF, LIFE...

Neurology · 75d

Cleared Jul 30, 2002

TTECH MODEL 200E + TENS DEVICE

Neurology · 85d