510(k) K880518 ยท OXO Image-Intensified Fluoroscopic X-Ray System, Mobile
MOBILE C-ARM OMNI 325
| Applicant | Fischer Imaging Corp., Denver CO, US |
| Decision | Substantially Equivalent, Mar 9, 1988 |
| Received | Feb 9, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K880518
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.