510(k) K952579 ยท HFM Monitor, Uterine Contraction, External (For Use In Clinic)
TOCO TRANSDUCER
| Applicant | Scientific Device Manufacturer, LLC, San Rafael CA, US |
| Decision | Substantially Equivalent, Aug 4, 1995 |
| Received | Jun 5, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K952579
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.