510(k) K893674 ยท IZO Generator, High-Voltage, X-Ray, Diagnostic
RME 325R
| Applicant | Fischer Imaging Corp., Denver CO, US |
| Decision | Substantially Equivalent, Jul 20, 1989 |
| Received | May 15, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K893674
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.