510(k) K933460 ยท IZI System, X-Ray, Angiographic
DVFX, MODEL M256
| Applicant | Xre Corp., Littleton MA, US |
| Decision | Substantially Equivalent, Apr 7, 1994 |
| Received | Jul 16, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K933460
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.