510(k) K970850 ยท EHD Unit, X-Ray, Extraoral With Timer
SCANRITE DFS
| Applicant | Scanrite Systems, Fremont CA, US |
| Decision | Substantially Equivalent, May 14, 1997 |
| Received | Mar 7, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K970850
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.