510(k) K926122 ยท JAA System, X-Ray, Fluoroscopic, Image-Intensified
FLUOREX
| Applicant | Toshiba America Medical Systems, In.C, Tustin CA, US |
| Decision | Substantially Equivalent, Feb 12, 1993 |
| Received | Dec 4, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K926122
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.