510(k) K120892 ยท DXT Injector And Syringe, Angiographic
DISPOSABLE 330PSI EXTENSION LINES
| Applicant | Coeur, Inc., Lebanon TN, US |
| Decision | Substantially Equivalent, Jun 10, 2013 |
| Received | Mar 23, 2012 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K120892
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.