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HeartBeam AIMIGo with 12-L ECG Synthesis Software System

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K250258
510(k) Type
Traditional
Applicant
Heartbeam, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/8/2025
Days to Decision
314 days
Submission Type
Summary

HeartBeam AIMIGo with 12-L ECG Synthesis Software System

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K250258
510(k) Type
Traditional
Applicant
Heartbeam, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/8/2025
Days to Decision
314 days
Submission Type
Summary