510(k) K191692 ยท DPS Electrocardiograph
KardioScreen
| Applicant | Imedrix Inc. (Formerly Piitech Inc.), Milpitas CA, US |
| Decision | Substantially Equivalent, Jan 10, 2020 |
| Received | Jun 25, 2019 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K191692
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.