510(k) K800613 ยท DXT Injector And Syringe, Angiographic
ANGIOPLASTY INJECTOR
| Applicant | Medrad, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Apr 8, 1980 |
| Received | Mar 18, 1980 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K800613
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.