510(k) K833138 ยท DXT Injector And Syringe, Angiographic
DIGITAL INJECTOR SYS
| Applicant | Sybron Corp., Mchenry IL, US |
| Decision | Substantially Equivalent, Nov 14, 1983 |
| Received | Sep 14, 1983 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K833138
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.