510(k) K013477 ยท HFM Monitor, Uterine Contraction, External (For Use In Clinic)
TOCO LITE, MODEL TD-01
| Applicant | Ventrex, Inc., Ventura CA, US |
| Decision | Substantially Equivalent, Jan 17, 2002 |
| Received | Oct 19, 2001 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K013477
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.