510(k) K161716 ยท KZM Device, Muscle Monitoring
TEETHAN 2.0
| Applicant | Bts S.P.A., Padova, IT |
| Decision | Substantially Equivalent, Dec 21, 2016 |
| Received | Jun 21, 2016 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K161716
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.