510(k) K072576 ยท FPA Set, Administration, Intravascular
CLEARLINK ANTIMICROBIAL LUER ACTIVATED DEVICE (LAD) AND EXTENSION SETS WITH THE CLEARLINK ANTIMICROBIAL LUER ACTIVATED
| Applicant | Baxter Healthcare Corp, Mcgaw Park IL, US |
| Decision | Substantially Equivalent, Nov 6, 2007 |
| Received | Sep 13, 2007 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K072576
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.