510(k) K903623 ยท HFM Monitor, Uterine Contraction, External (For Use In Clinic)
MODEL600 UTERINE ACTIVITY MONITOR
| Applicant | Corometrics Medical Systems, Inc., Wallingford CT, US |
| Decision | Substantially Equivalent, Nov 7, 1990 |
| Received | Aug 9, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K903623
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.