510(k) K062403 ยท MUH System, X-Ray, Extraoral Source, Digital
IMAX CEPH DIGITAL X-RAY SENSOR
| Applicant | Owandy, Ormond Beach FL, US |
| Decision | Substantially Equivalent, Nov 14, 2006 |
| Received | Aug 17, 2006 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K062403
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.