510(k) K081820 ยท DWF Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass
AVALON ELITE BI-CAVAL DUAL LUMEN CATHETER, 13FR, 16FR, 19FR, 20FR, 23FR, 27FR, 31FR
| Applicant | Avalon Laboratories, LLC, Austin TX, US |
| Decision | Substantially Equivalent, Oct 6, 2008 |
| Received | Jun 27, 2008 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K081820
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.