510(k) K141208 ยท LQW Test, Temperature Discrimination
DYNAMIC NEUROSCREENING DEVICE
| Applicant | Prosenex, Leola PA, US |
| Decision | Substantially Equivalent, Jul 23, 2014 |
| Received | May 9, 2014 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K141208
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.