510(k) K071774 ยท DTZ Oxygenator, Cardiopulmonary Bypass
JOSTRA QUADROX D DIFFUSION MEMBRANE OXYGENATOR WITH BIOLINE COATING, MODEL BE-HMOD 2000, BEQ-HMOD 2030
| Applicant | Maquet Cardiopulmonary, AG, Hirrlingen, DE |
| Decision | Substantially Equivalent, Jan 23, 2008 |
| Received | Jun 29, 2007 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K071774
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.