510(k) K882080 ยท HFM Monitor, Uterine Contraction, External (For Use In Clinic)
MODEL NUMBER (TBD) TOCO DATA TELEPHONE TRANS. SYS.
| Applicant | Aequitron Medical, Inc., Plymouth MN, US |
| Decision | Substantially Equivalent, Mar 1, 1989 |
| Received | May 17, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K882080
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.