510(k) K926233 ยท KRI Accessory Equipment, Cardiopulmonary Bypass
CARDIO2 CYCLE
| Applicant | Ergometrix, Inc., Minneapolis MN, US |
| Decision | Substantially Equivalent, Jun 4, 1993 |
| Received | Dec 11, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K926233
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.