510(k) K142769 ยท HEK Monitor, Heart Sound, Fetal, Ultrasonic
Fetal Doppler
| Applicant | Icare Newlife Technologies, Inc., Beijing, CN |
| Decision | Substantially Equivalent, Mar 20, 2015 |
| Received | Sep 25, 2014 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K142769
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.