510(k) K150902 ยท DXT Injector And Syringe, Angiographic
330psi Extension Y-Line with Dual Check Valve
| Applicant | Coeur, Inc., Lebanon TN, US |
| Decision | Substantially Equivalent, Oct 22, 2015 |
| Received | Apr 3, 2015 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K150902
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.