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Theratech, Inc.

5 FDA 510(k) clearances · Manufacturer

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RecordFirmDate
IF TRUE SINE INTERFERENTIAL STIMULATOR / MODEL WL-2206A1 & WI-2206A2 (K060975)Theratech, Inc.2006-05-10
IF TRUE SINE INTERFERENTIAL STIMULATOR, MODEL WL-2206A (K050847)Theratech, Inc.2005-06-17
IF SERIES TRUE SINE INTERFERENTIAL STIMULATOR/MODEL: WL-2206, WELL IF, LIFE IF AND THE CUSTOMER PRIVATE BRAND (K024100)Theratech, Inc.2003-02-25
TTECH MODEL 200E + TENS DEVICE (K021436)Theratech, Inc.2002-07-30
POWERED MUSCLE STIMULATOR (K013768)Theratech, Inc.2002-07-03

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Every clearance here is in the API, with alerts when new ones post.