510(k) K121758 ยท HGM System, Monitoring, Perinatal
CERNER FETALINK+(VERSION1.0)
| Applicant | Cerner Corp., Kansas City MO, US |
| Decision | Substantially Equivalent, Oct 9, 2012 |
| Received | Jun 15, 2012 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K121758
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.