510(k) K162951 ยท FPA Set, Administration, Intravascular
TUBETECH IV Administration Set
| Applicant | Douglas Medical Products, Inc., Mundelein IL, US |
| Decision | Substantially Equivalent, Jul 28, 2017 |
| Received | Oct 24, 2016 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K162951
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.