510(k) K944875 ยท DXT Injector And Syringe, Angiographic
ANGIOMAT 3000, 6000, CT INJECTOR
| Applicant | Lievel-Flarsheim Co., Oh OH, US |
| Decision | Substantially Equivalent, Jan 4, 1995 |
| Received | Oct 3, 1994 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K944875
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.