510(k) K912416 ยท IZI System, X-Ray, Angiographic
ANGIOGRAPHIC OR FLUOROSCOPIC X-RAY SYSTEM
| Applicant | Xre Corp., Littleton MA, US |
| Decision | Substantially Equivalent, Aug 28, 1991 |
| Received | May 31, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K912416
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.