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HeartBeam AIMIGo(TM) System

Page Type
Cleared 510(K)
510(k) Number
K231424
510(k) Type
Traditional
Applicant
Heartbeam, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/13/2024
Days to Decision
576 days
Submission Type
Summary

HeartBeam AIMIGo(TM) System

Page Type
Cleared 510(K)
510(k) Number
K231424
510(k) Type
Traditional
Applicant
Heartbeam, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/13/2024
Days to Decision
576 days
Submission Type
Summary