510(k) K060328 ยท MUH System, X-Ray, Extraoral Source, Digital
PLANMECA PROMAX 3D
| Applicant | Planmeca Oy, Helsinki, FI |
| Decision | Substantially Equivalent, Mar 15, 2006 |
| Received | Feb 9, 2006 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K060328
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.