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ALIVECOR HEART MONITOR

Page Type
Cleared 510(K)
510(k) Number
K130409
510(k) Type
Traditional
Applicant
ALIVECOR, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/6/2013
Days to Decision
199 days
Submission Type
Statement

ALIVECOR HEART MONITOR

Page Type
Cleared 510(K)
510(k) Number
K130409
510(k) Type
Traditional
Applicant
ALIVECOR, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/6/2013
Days to Decision
199 days
Submission Type
Statement