Last synced on 16 May 2025 at 11:05 pm

ALIVECOR HEART MONITOR

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