510(k) K902983 ยท JAA System, X-Ray, Fluoroscopic, Image-Intensified
SIEMEN'S SIREMOBILE II C-ARM
| Applicant | Electromek Diagnostic Systems, Inc., Troy IL, US |
| Decision | Substantially Equivalent, Nov 6, 1990 |
| Received | Jun 26, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K902983
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.