510(k) K133351 ยท FPA Set, Administration, Intravascular
NEXUS NIS-6P LUER ACTIVATED DEVICE
| Applicant | Nexus Medical, LLC, Lenexa KS, US |
| Decision | Substantially Equivalent, May 22, 2014 |
| Received | Oct 31, 2013 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K133351
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.