510(k) K933447 ยท OXO Image-Intensified Fluoroscopic X-Ray System, Mobile
STENOSCOP MOBILE FLUOROSCOPIC XRAY SYSTEM
| Applicant | GE Medical Systems, Milwaukee WI, US |
| Decision | Substantially Equivalent, Aug 23, 1993 |
| Received | Jul 13, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K933447
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.