510(k) K895730 ยท JAA System, X-Ray, Fluoroscopic, Image-Intensified
X-RAY EQUIPMENT (VARIOUS TYPES)
| Applicant | Continental X-Ray Corp., Chicago IL, US |
| Decision | Substantially Equivalent, Nov 6, 1989 |
| Received | Sep 22, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K895730
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.