510(k) K093590 ยท MUH System, X-Ray, Extraoral Source, Digital
PLANMECA PROMAX 3D MAX
| Applicant | Planmeca Oy, Helsinki, FI |
| Decision | Substantially Equivalent, May 12, 2010 |
| Received | Nov 19, 2009 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K093590
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.