510(k) K181823 ยท DQK Computer, Diagnostic, Programmable
KardiaAI
| Applicant | AliveCor, Inc., Mountain View CA, US |
| Decision | Substantially Equivalent, Mar 11, 2019 |
| Received | Jul 9, 2018 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K181823
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.