510(k) K033247 ยท DXT Injector And Syringe, Angiographic
MEDRAD SPECTRIS SOLARIS MR INJECTOR SYSTEM
| Applicant | Medrad, Inc., Indianola PA, US |
| Decision | Substantially Equivalent, Nov 5, 2003 |
| Received | Oct 7, 2003 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K033247
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.