510(k) K061044 ยท HFM Monitor, Uterine Contraction, External (For Use In Clinic)
FEATHERLITE AQUA TOCODYNAMOMETER
| Applicant | Ventrex, Inc., Ventura CA, US |
| Decision | Substantially Equivalent, Jul 12, 2006 |
| Received | Apr 14, 2006 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K061044
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.