510(k) K113398 ยท FPA Set, Administration, Intravascular
NEXUS TKO-6, LUER-ACTIVATED DEVICE
| Applicant | Nexus Medical, LLC, Lenexa KS, US |
| Decision | Substantially Equivalent, Apr 18, 2012 |
| Received | Nov 17, 2011 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K113398
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.