510(k) K080738 ยท EAP Unit, X-Ray, Intraoral
DENTRON SENSOR
| Applicant | Dentron Systems, LLC, Ormond Beach FL, US |
| Decision | Substantially Equivalent, May 13, 2008 |
| Received | Mar 17, 2008 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K080738
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.