510(k) K131963 ยท FMF Syringe, Piston
TAUTONA INJECTOR DEVICE
| Applicant | Tautona Group, LLC, Menlo Park CA, US |
| Decision | Substantially Equivalent, Oct 22, 2013 |
| Received | Jun 27, 2013 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K131963
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.