510(k) K953582 ยท IZO Generator, High-Voltage, X-Ray, Diagnostic
HFX350, 30KW, 300MA, 1 OR 3 PHASE RADIOGRAPHIC & FLUOROSCOPIC X-RAY GENERATOR
| Applicant | Varian Canada, Inc., Canada L7g 2j4, CA |
| Decision | Substantially Equivalent, Sep 26, 1995 |
| Received | Aug 1, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K953582
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.