510(k) K253838 ยท DTZ Oxygenator, Cardiopulmonary Bypass
Lifemotion Disposable Membrane Oxygenator
| Applicant | Lifemotion Medical Technology Co., Ltd., Shenzhen, CN |
| Decision | Substantially Equivalent, Mar 16, 2026 |
| Received | Dec 1, 2025 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K253838
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.