510(k) K911931 ยท FPA Set, Administration, Intravascular
LUER LOCK INJECTION CAP
| Applicant | Dmd Products, Nevada City CA, US |
| Decision | Substantially Equivalent, Jun 18, 1991 |
| Received | Apr 30, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K911931
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.