510(k) K133265 ยท KFM Pump, Blood, Cardiopulmonary Bypass, Non-Roller Type
QUADROX-IR ADULT AND SMALL ADULT
| Applicant | Maquet Cardiopulmonary, AG, Wayne NJ, US |
| Decision | Substantially Equivalent, Nov 12, 2013 |
| Received | Oct 23, 2013 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K133265
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.