510(k) K911739 ยท OXO Image-Intensified Fluoroscopic X-Ray System, Mobile
SWEMAC REISON BIPLANAR 300
| Applicant | Seemac Reison AB Co., Sweden, SE |
| Decision | Substantially Equivalent, Oct 23, 1991 |
| Received | Apr 17, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K911739
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.