510(k) K992559 ยท DTZ Oxygenator, Cardiopulmonary Bypass
HOLLOW FIBER MEMBRANE OYGENATOR QUADROX HMO 1010
| Applicant | Jostra Bentley, Newark DE, US |
| Decision | Substantially Equivalent, Sep 20, 1999 |
| Received | Jul 30, 1999 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K992559
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.