510(k) K823920 ยท DXT Injector And Syringe, Angiographic
COEURLOCK STERILE DISPOS. ANGIOGRAPHIC
| Applicant | Coeur Laboratories, Inc. NC, US |
| Decision | Substantially Equivalent, Feb 18, 1983 |
| Received | Dec 28, 1982 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K823920
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.