510(k) K063600 ยท JAF Monitor, Ultrasonic, Nonfetal
VISTA AVS
| Applicant | Summit Doppler Systems, Inc., Golden CO, US |
| Decision | Substantially Equivalent, Dec 19, 2006 |
| Received | Dec 4, 2006 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K063600
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.