510(k) K880982 ยท KPR System, X-Ray, Stationary
ORALIX PAN DC III CEPH OR PANORAMIC MODE ONLY
| Applicant | Orion Corporation Soredex, Helsinki, FI |
| Decision | Substantially Equivalent, Jun 6, 1988 |
| Received | Mar 8, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K880982
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.