510(k) K013944 ยท DWF Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass
JOSTRA DUAL STAGE VENOUS RETURN CANNULAE
| Applicant | Jostra AG, Oxford PA, US |
| Decision | Substantially Equivalent, Feb 11, 2002 |
| Received | Nov 29, 2001 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K013944
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.