510(k) K131923 ยท GZI Stimulator, Neuromuscular, External Functional
NEURODYN PORTABLE TENS NFES, NEURODYN PORTABLE TENS
| Applicant | Techlink International, Miami FL, US |
| Decision | Substantially Equivalent, Jul 3, 2014 |
| Received | Jun 26, 2013 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K131923
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.