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Theratech, Inc.

FDA 510(k) & PMA Approved Devices — 5 products

Total Devices5
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K060975 IF TRUE SINE INTERFERENTIAL STIMULATOR / MODEL WL-2206A1 & WI-2206A2LIH2006-05-10 View
510(k) K050847 IF TRUE SINE INTERFERENTIAL STIMULATOR, MODEL WL-2206AIPF2005-06-17 View
510(k) K024100 IF SERIES TRUE SINE INTERFERENTIAL STIMULATOR/MODEL: WL-2206, WELL IF, LIFE IF AND THE CUSTOMER PRIVATE BRANDLIH2003-02-25 View
510(k) K021436 TTECH MODEL 200E + TENS DEVICEGZJ2002-07-30 View
510(k) K013768 POWERED MUSCLE STIMULATORIPF2002-07-03 View
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