510(k) K883431 ยท IZO Generator, High-Voltage, X-Ray, Diagnostic
RAYMAX 2100 MODELS 2130 & 2136
| Applicant | Raymax Medical Corp., Ontario, L4l 7k5, CA |
| Decision | Substantially Equivalent, Sep 12, 1988 |
| Received | Aug 15, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K883431
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.