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ALIVECOR HEART MONITOR OTC

Page Type
Cleared 510(K)
510(k) Number
K130921
510(k) Type
Traditional
Applicant
ALIVECOR, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/6/2014
Days to Decision
309 days
Submission Type
Statement

ALIVECOR HEART MONITOR OTC

Page Type
Cleared 510(K)
510(k) Number
K130921
510(k) Type
Traditional
Applicant
ALIVECOR, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/6/2014
Days to Decision
309 days
Submission Type
Statement