510(k) K070798 ยท DXT Injector And Syringe, Angiographic
ADAPTERS FOR CT, ANGIOGRAPHIC, AND/OR MRI POWER INJECTORS
| Applicant | Coeur, Inc., Lebanon TN, US |
| Decision | Substantially Equivalent, Oct 4, 2007 |
| Received | Mar 23, 2007 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K070798
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.