510(k) K894030 ยท HFM Monitor, Uterine Contraction, External (For Use In Clinic)
MODEL 37 UTERINE CONTRACTION ACTIVITY MONITOR
| Applicant | Healthdyne, Inc., Marietta GA, US |
| Decision | Substantially Equivalent, Jan 22, 1990 |
| Received | Jun 6, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K894030
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.