510(k) K092382 ยท FPA Set, Administration, Intravascular
NEXUS PRESSURE RATED EXTENSION SETS
| Applicant | Nexus Medical, LLC, Lenexa KS, US |
| Decision | Substantially Equivalent, Apr 26, 2010 |
| Received | Aug 5, 2009 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K092382
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.