510(k) K011991 ยท DXT Injector And Syringe, Angiographic
MODIFICATION TO MEDRAD SPECTRIS MR INJECTOR
| Applicant | Medrad, Inc., Indianola PA, US |
| Decision | Substantially Equivalent, Aug 21, 2001 |
| Received | Jun 26, 2001 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K011991
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.