510(k) K130723 ยท NGX Stimulator, Muscle, Powered, For Muscle Conditioning
FDES106 MINI TENS&EMS DEVICE,FDES106 MULTI-FUNCTION MINI TENS&EMS DEVICE,FDES105 PAIN RELIEF PLASTER,FDES107 ABDOMINAL
| Applicant | Famidoc Technology Co., Ltd., Dongguan, CN |
| Decision | Substantially Equivalent, Feb 7, 2014 |
| Received | Mar 18, 2013 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K130723
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.