510(k) K123868 ยท FPA Set, Administration, Intravascular
INTERLINK SYSTEM LEVER LOCK CANNULA WITH CHECK VALVE, SECONDARY MEDICATION SETS, SOLUTION SETS, CONTINU-FLO SOLUTION SET
| Applicant | Baxter Healthcare Corp, Round Lake IL, US |
| Decision | Substantially Equivalent, Jan 8, 2013 |
| Received | Dec 17, 2012 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K123868
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.