510(k) K834107 ยท DXT Injector And Syringe, Angiographic
ANGIOPLASTY INFLATION DEVICE & CARTR
| Applicant | Cordis Corp., Mchenry IL, US |
| Decision | Substantially Equivalent, Jan 13, 1984 |
| Received | Nov 29, 1983 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K834107
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.