510(k) K961690 ยท JAA System, X-Ray, Fluoroscopic, Image-Intensified
CARDIOARC SERIES: POSITIONER C-ARM MODELS NO. 6896.001 AND 6896.105
| Applicant | Continental X-Ray Corp., Broadview IL, US |
| Decision | Substantially Equivalent, Jun 27, 1996 |
| Received | May 1, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K961690
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.