510(k) K012950 ยท DXT Injector And Syringe, Angiographic
MODIFICATION TO: MEDRAD SPECTRIS SOLARIS MR INJECTOR SYSTEM
| Applicant | Medrad, Inc., Indianola PA, US |
| Decision | Substantially Equivalent, Oct 4, 2001 |
| Received | Sep 4, 2001 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K012950
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.