510(k) K893770 ยท HFM Monitor, Uterine Contraction, External (For Use In Clinic)
TERM GUARD II DEVICE
| Applicant | Tokos Medical Corp., Santa Ana CA, US |
| Decision | Substantially Equivalent, Nov 3, 1989 |
| Received | May 22, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K893770
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.