510(k) K022321 ยท DWF Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass
STOCKERT V172-28 VENOUS FEMORAL CANNULA
| Applicant | Stockert Instrumente GmbH, Arvada CO, US |
| Decision | Substantially Equivalent, Oct 9, 2002 |
| Received | Jul 17, 2002 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K022321
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.