510(k) K161808 ยท FPA Set, Administration, Intravascular
Solution Set with 1.2 Micron Air Eliminating Filter
| Applicant | Baxter Healthcare Corporation, Round Lake IL, US |
| Decision | Substantially Equivalent, Jun 21, 2017 |
| Received | Jul 1, 2016 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K161808
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.