510(k) K030264 ยท DTZ Oxygenator, Cardiopulmonary Bypass
QUANDROX SAFELINE HOLLOW FIBER MEMBRANE OXYGENATOR, MODEL HMO 2030
| Applicant | Jostra AG, Hirrlingen, DE |
| Decision | Substantially Equivalent, Feb 26, 2003 |
| Received | Jan 27, 2003 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K030264
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.