510(k) K121032 ยท FPA Set, Administration, Intravascular
PRIMARY SYMBIQ SET, DITAL MICROBORE TUBING, 0.2 MICRON FILTER, NON-DEHP
| Applicant | Hospira, Inc., Lake Forest IL, US |
| Decision | Substantially Equivalent, Jun 21, 2012 |
| Received | Apr 5, 2012 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K121032
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.