510(k) K880522 ยท IZO Generator, High-Voltage, X-Ray, Diagnostic
THREE PHASE, DIAGNOSTIC X-RAY GENERATOR MICRO-X 80
| Applicant | Fischer Imaging Corp., Denver CO, US |
| Decision | Substantially Equivalent, May 4, 1988 |
| Received | Feb 9, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K880522
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.