510(k) K220842 ยท KFM Pump, Blood, Cardiopulmonary Bypass, Non-Roller Type
Quantum Perfusion Centrifugal Blood Pump CP22 with Integrated Sensors, Quantum Perfusion Centrifugal Blood Pump CP20 with Integrated Sensors
| Applicant | Qura S.R.L, Mirandola, IT |
| Decision | Substantially Equivalent, May 19, 2023 |
| Received | Mar 23, 2022 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K220842
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.