510(k) K833078 ยท DTZ Oxygenator, Cardiopulmonary Bypass
HOLLOW FIBER MEMBRANE OXYGENATOR-HF4000
| Applicant | Cordis Corp., Mchenry IL, US |
| Decision | Substantially Equivalent, Jan 27, 1984 |
| Received | Sep 9, 1983 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K833078
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.