510(k) K133261 ยท DTZ Oxygenator, Cardiopulmonary Bypass
MEDOS HILITE 7000 & 7000 LT OXYGENATOR
| Applicant | Medos Medizintechnik AG, Ann Arbor MI, US |
| Decision | Substantially Equivalent, Jan 9, 2014 |
| Received | Oct 23, 2013 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K133261
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.