510(k) K000454 ยท MUH System, X-Ray, Extraoral Source, Digital
DIMEX 2
| Applicant | Planmeca Oy, Wood Dale IL, US |
| Decision | Substantially Equivalent, Mar 31, 2000 |
| Received | Feb 11, 2000 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K000454
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.