510(k) K001961 ยท DWF Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass
STOCKERT A242 AND A252 SERIES ARTERIAL FEMORAL CANNULAE
| Applicant | Stoeckert Instrumente, Arvada CO, US |
| Decision | Substantially Equivalent, Jan 25, 2001 |
| Received | Jun 27, 2000 |
| Type | Abbreviated |
| FDA record | Open on fda.gov |
Recalls that name K001961
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.