510(k) K880877 ยท DXT Injector And Syringe, Angiographic
CONTRAST INJECTION DEVICE
| Applicant | Med-West, Inc., Salt Lake City UT, US |
| Decision | Substantially Equivalent, May 31, 1988 |
| Received | Mar 1, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K880877
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.