510(k) K900034 ยท DXT Injector And Syringe, Angiographic
ANGIO-MAX
| Applicant | Accumed Systems, Inc., Shaker Heights OH, US |
| Decision | Substantially Equivalent, May 22, 1990 |
| Received | Jan 2, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K900034
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.