510(k) K162023 ยท DQK Computer, Diagnostic, Programmable
CardioDay V2.5
| Applicant | Getemed Medizin- Und Informationstechnik AG, Teltow, DE |
| Decision | Substantially Equivalent, Mar 24, 2017 |
| Received | Jul 22, 2016 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K162023
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.