510(k) K864837 ยท JAA System, X-Ray, Fluoroscopic, Image-Intensified
MODIFIED MAINFRAME OF MODEL 902 MOBILE C-ARM
| Applicant | Oec-Diasonics, Inc., Salt Lake City UT, US |
| Decision | Substantially Equivalent, Jan 30, 1987 |
| Received | Dec 9, 1986 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K864837
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.