510(k) K012325 ยท KFM Pump, Blood, Cardiopulmonary Bypass, Non-Roller Type
CARDIOVENTION CORX SYSTEM, MODEL FG 0001
| Applicant | Cardiovention, Inc., Santa Clara CA, US |
| Decision | Substantially Equivalent, Apr 9, 2002 |
| Received | Jul 23, 2001 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K012325
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.