Theratech, Inc.
FDA 510(k) medical device clearances.
Top product codes for Theratech, Inc.
Recent clearances by Theratech, Inc.
- K060975 — IF TRUE SINE INTERFERENTIAL STIMULATOR / MODEL WL-2206A1 & WI-2206A2
- K050847 — IF TRUE SINE INTERFERENTIAL STIMULATOR, MODEL WL-2206A
- K024100 — IF SERIES TRUE SINE INTERFERENTIAL STIMULATOR/MODEL: WL-2206, WELL IF, LIFE IF AND THE CUSTOMER PRIVATE BRAND
- K021436 — TTECH MODEL 200E + TENS DEVICE
- K013768 — POWERED MUSCLE STIMULATOR
Data sourced from openFDA. This site is unofficial and independent of the FDA.