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AliveCor Heart Monitor

Page Type
Cleared 510(K)
510(k) Number
K142672
510(k) Type
Special
Applicant
ALIVECOR, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/3/2014
Days to Decision
75 days
Submission Type
Summary

AliveCor Heart Monitor

Page Type
Cleared 510(K)
510(k) Number
K142672
510(k) Type
Special
Applicant
ALIVECOR, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/3/2014
Days to Decision
75 days
Submission Type
Summary