510(k) K902104 ยท HFM Monitor, Uterine Contraction, External (For Use In Clinic)
ORION WATCHGUARD
| Applicant | Orion Industries, Fort Myers FL, US |
| Decision | Substantially Equivalent, Oct 25, 1990 |
| Received | May 8, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K902104
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.