510(k) K932445 ยท JAA System, X-Ray, Fluoroscopic, Image-Intensified
SIRESKOP CX
| Applicant | Siemens Medical Solutions USA, Inc., Iselin NJ, US |
| Decision | Substantially Equivalent, Sep 7, 1993 |
| Received | May 20, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K932445
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.