510(k) K222902 ยท DPS Electrocardiograph
Electrocardiograph: SE-1200 Pro and SE-1201 Pro
| Applicant | Edan Instruments, Inc., Shenzhen, CN |
| Decision | Substantially Equivalent, Jul 28, 2023 |
| Received | Sep 23, 2022 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K222902
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.