510(k) K911562 ยท IZO Generator, High-Voltage, X-Ray, Diagnostic
EDITOR MP 800/HF-850 X-RAY CONTROL AND GENERATOR
| Applicant | Continental X-Ray Corp., Broadview IL, US |
| Decision | Substantially Equivalent, Oct 24, 1991 |
| Received | Apr 8, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K911562
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.