510(k) K081933 ยท DWF Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass
AVALON ELITE MULTI-PORT VENOUS FEMORAL CATHETER, 20FR, 22FR, 24FR, 26FR, 28FR
| Applicant | Avalon Laboratories, LLC, Rancho Dominguez CA, US |
| Decision | Substantially Equivalent, Oct 3, 2008 |
| Received | Jul 7, 2008 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K081933
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.