510(k) K093393 ยท JAF Monitor, Ultrasonic, Nonfetal
LIFEDOP MODEL 300ABI
| Applicant | Summit Doppler Systems, Inc., Golden CO, US |
| Decision | Substantially Equivalent, Dec 24, 2009 |
| Received | Oct 30, 2009 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K093393
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.