510(k) K800639 ยท JAA System, X-Ray, Fluoroscopic, Image-Intensified
ORBITOR
| Applicant | Philips Medical Systems (Cleveland), Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, May 14, 1980 |
| Received | Mar 24, 1980 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K800639
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.