510(k) K081289 ยท FPA Set, Administration, Intravascular
V-LINK ANTIMICROBIAL LUER ACTIVATED DEVICE AND EXTENSION SETS WITH V-LINK ANTIMICROBIAL LUER ACTIVATED DEVICE
| Applicant | Baxter Healthcare Corp, Mcgaw Park IL, US |
| Decision | Substantially Equivalent, Aug 4, 2008 |
| Received | May 7, 2008 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K081289
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.