510(k) K842422 ยท HGM System, Monitoring, Perinatal
KONTRON FAX FETAL MONITOR
| Applicant | Kontron Instruments, Inc., Walker MI, US |
| Decision | Substantially Equivalent, Sep 20, 1985 |
| Received | Jun 20, 1984 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K842422
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.