510(k) K902221 ยท DXT Injector And Syringe, Angiographic
MODIFIED ANGIOGRAPHIC INJECTOR AND SYRINGE
| Applicant | Mallinckrodt Group, Inc., Cincinnati OH, US |
| Decision | Substantially Equivalent, Aug 8, 1990 |
| Received | May 17, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K902221
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.