510(k) K972312 ยท EHD Unit, X-Ray, Extraoral With Timer
SIEMENS ORTHOPHOS DS/DS CEPH
| Applicant | Siemens AG, North Attleboro MA, US |
| Decision | Substantially Equivalent, Sep 15, 1997 |
| Received | Jun 20, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K972312
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.