Theratech, Inc.
Theratech, Inc. appears in FDA public data with 0 recalls, 5 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on May 10, 2006.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 5
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K060975 | IF TRUE SINE INTERFERENTIAL STIMULATOR / MODEL WL-2206A1 & WI-2206A2 | May 10, 2006 |
| K050847 | IF TRUE SINE INTERFERENTIAL STIMULATOR, MODEL WL-2206A | June 17, 2005 |
| K024100 | IF SERIES TRUE SINE INTERFERENTIAL STIMULATOR/MODEL: WL-2206, WELL IF, LIFE IF AND THE CUSTOMER PRIV | February 25, 2003 |
| K021436 | TTECH MODEL 200E + TENS DEVICE | July 30, 2002 |
| K013768 | POWERED MUSCLE STIMULATOR | July 3, 2002 |