510(k) K233702 ยท DWE Tubing, Pump, Cardiopulmonary Bypass
SMARxT Tubing and Connectors
| Applicant | LivaNova USA, Inc., Arvada CO, US |
| Decision | Substantially Equivalent, Aug 8, 2024 |
| Received | Nov 17, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K233702
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.