510(k) K131889 ยท OSP Uterine Electromyographic Monitor
EUM 100PRO
| Applicant | Promedic, Inc., Bonita Springs FL, US |
| Decision | Substantially Equivalent, Apr 23, 2014 |
| Received | Jun 25, 2013 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K131889
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.