510(k) K953832 ยท KPR System, X-Ray, Stationary
SOLARIX FV
| Applicant | GE Medical Systems, Milwaukee WI, US |
| Decision | Substantially Equivalent, Sep 12, 1995 |
| Received | Aug 16, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K953832
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.