510(k) K161036 ยท FPA Set, Administration, Intravascular
Hospira Extension Set, Hospira Primary Set
| Applicant | Hospira, Inc., Lake Forest IL, US |
| Decision | Substantially Equivalent, Jan 6, 2017 |
| Received | Apr 13, 2016 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K161036
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.