ClearanceBrief
510(k) K220350 ยท DXH Transmitters And Receivers, Electrocardiograph, Telephone

KardiaMobile 6L

ApplicantAliveCor, Inc., Mountain View CA, US
DecisionSubstantially Equivalent, May 25, 2022
ReceivedFeb 7, 2022
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K220350

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.