510(k) K001509 ยท DWF Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass
STOCKERT V172 SERIES VENOUS FEMORAL CANNULAE
| Applicant | Cobe Cardiovascular, Inc., Arvada CO, US |
| Decision | Substantially Equivalent, Oct 26, 2001 |
| Received | May 15, 2000 |
| Type | Abbreviated |
| FDA record | Open on fda.gov |
Recalls that name K001509
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.