510(k) K863537 ยท DXT Injector And Syringe, Angiographic
CORDIS REUSABLE INFLATION DEVICE FOR ANGIOPLASTY
| Applicant | Cordis Corp., Miami FL, US |
| Decision | Substantially Equivalent, Oct 31, 1986 |
| Received | Sep 11, 1986 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K863537
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.