510(k) K970263 ยท EHD Unit, X-Ray, Extraoral With Timer
PM 2002 CC PROLINE
| Applicant | Planmeca Oy, Helsinki, FI |
| Decision | Substantially Equivalent, Feb 26, 1997 |
| Received | Jan 23, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K970263
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.