510(k) K142545 ยท LKF Cannula, Manipulator/Injector, Uterine
SonoFlow Sonohysterography and Sonohysterosalpingography Device
| Applicant | Crossbay Medical, Inc., Hayward CA, US |
| Decision | Substantially Equivalent, Mar 20, 2015 |
| Received | Sep 10, 2014 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K142545
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.