510(k) K160870 ยท FPA Set, Administration, Intravascular
Hospira Administration Sets
| Applicant | Hospira, Inc., Lake Forest IL, US |
| Decision | Substantially Equivalent, Jun 1, 2016 |
| Received | Mar 30, 2016 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K160870
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.