510(k) K883976 ยท IZO Generator, High-Voltage, X-Ray, Diagnostic
CFX 625
| Applicant | Fischer Imaging Corp., Denver CO, US |
| Decision | Substantially Equivalent, Dec 13, 1988 |
| Received | Sep 20, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K883976
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.