510(k) K120443 ยท FPA Set, Administration, Intravascular
NEUTRAL LUER ACTIVATED DEVICE AND EXTENSION SETS WITH NEUTRAL LUER ACTIVATED DEVICE
| Applicant | Baxter Healthcare Corporation - Renal Division, Mcgaw Park IL, US |
| Decision | Substantially Equivalent, May 22, 2012 |
| Received | Feb 14, 2012 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K120443
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.