510(k) K890292 ยท DXT Injector And Syringe, Angiographic
PCA-10, 10CC DISP. ANGIOGRAPHY CONTROL SYRINGE
| Applicant | Coeur Laboratories, Inc., Raleigh NC, US |
| Decision | Substantially Equivalent, Jun 22, 1989 |
| Received | Jan 19, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K890292
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.