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Samsung ECG Monitor Application with Irregular Heart Rhythm Notification

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K230292
510(k) Type
Traditional
Applicant
Samsung Electronics Co., Ltd.
Country
South Korea
FDA Decision
Substantially Equivalent
Decision Date
5/2/2023
Days to Decision
89 days
Submission Type
Summary

Samsung ECG Monitor Application with Irregular Heart Rhythm Notification

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K230292
510(k) Type
Traditional
Applicant
Samsung Electronics Co., Ltd.
Country
South Korea
FDA Decision
Substantially Equivalent
Decision Date
5/2/2023
Days to Decision
89 days
Submission Type
Summary