510(k) K951765 ยท OXO Image-Intensified Fluoroscopic X-Ray System, Mobile
SERIES 6600 DIGITAL MOBILE C-ARM
| Applicant | Ge Dec Medical Systems, Salt Lake City UT, US |
| Decision | Substantially Equivalent, May 11, 1995 |
| Received | Apr 17, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K951765
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.