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ALIVECOR HEART MONITOR OTC

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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