510(k) K983270 ยท DWF Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass
VOYAGER QUAD CANNULA
| Applicant | Cardiothoracic Systems, Inc., Cupertino CA, US |
| Decision | Substantially Equivalent, Jul 28, 1999 |
| Received | Sep 17, 1998 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K983270
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.