510(k) K991783 ยท KFM Pump, Blood, Cardiopulmonary Bypass, Non-Roller Type
AB-180 XC SYSTEM, MODEL AB-180XC
| Applicant | Cardiacassist, Inc., Pittsburgh PA, US |
| Decision | Substantially Equivalent, Nov 1, 2000 |
| Received | May 25, 1999 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K991783
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.