510(k) K802953 ยท JAA System, X-Ray, Fluoroscopic, Image-Intensified
DIGITAL FLUOROGRAPHIC X-RAY SYSTEM
| Applicant | General Electric Co., Mchenry IL, US |
| Decision | Substantially Equivalent, Jan 9, 1981 |
| Received | Nov 20, 1980 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K802953
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.