510(k) K142367 ยท FPA Set, Administration, Intravascular
Hospira Primary Sets
| Applicant | Hospira, Inc., Lake Forest IL, US |
| Decision | Substantially Equivalent, Nov 25, 2014 |
| Received | Aug 25, 2014 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K142367
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Sep 11, 2026 | ICU Medical, Inc. IV Sets with drip chambers Open, Classified |
FPA | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.