510(k) K022174 ยท DWF Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass
MODIFICATION TO CARDEON AEGIS CATHETER
| Applicant | Cardeon Corp., Cupertino CA, US |
| Decision | Substantially Equivalent, Jul 29, 2002 |
| Received | Jul 3, 2002 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K022174
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.