510(k) K232721 ยท DTE Pulse-Generator, Pacemaker, External
Lifetech Cardio Temporary Pacemaker
| Applicant | Shenzhen Lifetech Cardio Medical Electronics Co., Ltd., Shenzhen, CN |
| Decision | Substantially Equivalent, Jan 7, 2024 |
| Received | Sep 5, 2023 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K232721
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.