510(k) K050692 ยท JAA System, X-Ray, Fluoroscopic, Image-Intensified
FLXIS
| Applicant | Philips Medical Systems North America Co., Bothell WA, US |
| Decision | Substantially Equivalent, Apr 8, 2005 |
| Received | Mar 17, 2005 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K050692
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.