510(k) K880525 ยท IZO Generator, High-Voltage, X-Ray, Diagnostic
3 PHASE HIGH FREQ. DIAG. X-RAY GEN. MICRO-X 60HF
| Applicant | Fischer Imaging Corp., Denver CO, US |
| Decision | Substantially Equivalent, Aug 15, 1988 |
| Received | Feb 9, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K880525
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.