510(k) K091251 ยท HGM System, Monitoring, Perinatal
CERNER FETALINK (VERSION 1.0)
| Applicant | Cerner Corp., Kansas City MO, US |
| Decision | Substantially Equivalent, Aug 25, 2009 |
| Received | Apr 29, 2009 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K091251
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.