510(k) K023132 ยท KFM Pump, Blood, Cardiopulmonary Bypass, Non-Roller Type
JOSTRA MECC SYSTEM
| Applicant | Jostra AG, The Woodlands TX, US |
| Decision | Substantially Equivalent, Dec 17, 2002 |
| Received | Sep 20, 2002 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K023132
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.