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ALIVECOR HEART MONITOR FOR IPHONE

Page Type
Cleared 510(K)
510(k) Number
K122356
510(k) Type
Traditional
Applicant
ALIVECOR, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/19/2012
Days to Decision
108 days
Submission Type
Statement

ALIVECOR HEART MONITOR FOR IPHONE

Page Type
Cleared 510(K)
510(k) Number
K122356
510(k) Type
Traditional
Applicant
ALIVECOR, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/19/2012
Days to Decision
108 days
Submission Type
Statement