510(k) K051664 ยท MUH System, X-Ray, Extraoral Source, Digital
SCAN300FP / RETROPAN (VDC)
| Applicant | Oy Ajat, Ltd., Ormond Beach FL, US |
| Decision | Substantially Equivalent, Jul 20, 2005 |
| Received | Jun 22, 2005 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K051664
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.