510(k) K230834 ยท DPS Electrocardiograph
CARDIPIA ECG / Model: CARDIPIA400H, CARDIPIA800H
| Applicant | Trismed Co., Ltd., Daejeon, KR |
| Decision | Substantially Equivalent, Nov 21, 2023 |
| Received | Mar 27, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K230834
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.