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HeartCheck Cardi Beat ECG Monitor with GEMS Mobile

Page Type
Cleared 510(K)
510(k) Number
K181310
510(k) Type
Traditional
Applicant
CardioComm Solutions, Inc.
Country
Canada
FDA Decision
Substantially Equivalent
Decision Date
2/22/2019
Days to Decision
281 days
Submission Type
Summary

HeartCheck Cardi Beat ECG Monitor with GEMS Mobile

Page Type
Cleared 510(K)
510(k) Number
K181310
510(k) Type
Traditional
Applicant
CardioComm Solutions, Inc.
Country
Canada
FDA Decision
Substantially Equivalent
Decision Date
2/22/2019
Days to Decision
281 days
Submission Type
Summary