510(k) K161323 ยท FPA Set, Administration, Intravascular
Solution Set for Epidural Use
| Applicant | Baxter Healthcare Corporation, Round Lake IL, US |
| Decision | Substantially Equivalent, Nov 30, 2016 |
| Received | May 11, 2016 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K161323
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.