510(k) K121634 ยท FPA Set, Administration, Intravascular
INTERLINK SYSTEM EXTENSION SET WITH CONTROL-A-FLO-REGULATORY CLEARLINK SYSTEM EXTENSION SET WITH CONTROL-A-FLO-REGULATOR
| Applicant | Baxter Healthcare Corporation, Round Lake IL, US |
| Decision | Substantially Equivalent, Jun 29, 2012 |
| Received | Jun 4, 2012 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K121634
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.