510(k) K103689 ยท MUH System, X-Ray, Extraoral Source, Digital
PLANMECA PROMAX 3D MID
| Applicant | Planmeca Oy, Helsinki, FI |
| Decision | Substantially Equivalent, Mar 17, 2011 |
| Received | Dec 17, 2010 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K103689
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.