510(k) K954847 ยท HFM Monitor, Uterine Contraction, External (For Use In Clinic)
DISCO UTERINE CONTRACTION TRANSDUCER & ACCESSORIES
| Applicant | Ocg Systems, Inc., Highland Park IL, US |
| Decision | Substantially Equivalent, May 22, 1996 |
| Received | Oct 23, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K954847
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.