510(k) K130002 ยท OSP Uterine Electromyographic Monitor
SURECALL LABOR MONITOR
| Applicant | Reproductive Research Technologies, LP, Houston TX, US |
| Decision | Substantially Equivalent, Jun 28, 2013 |
| Received | Jan 2, 2013 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K130002
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.