510(k) K042784 ยท DXT Injector And Syringe, Angiographic
MEDRAD SPECTRIS SOLARIS EP MR INJECTOR SYSTEM
| Applicant | Medrad, Inc., Indianola PA, US |
| Decision | Substantially Equivalent, Dec 10, 2004 |
| Received | Oct 6, 2004 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K042784
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.