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Reveal LINQ Insertable Cardiac Monitor, LINQ II Insertable Cardiac Monitor, AccuRhythm AI ECG Classification System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K223630
510(k) Type
Traditional
Applicant
Medtronic, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/5/2023
Days to Decision
121 days
Submission Type
Summary

Reveal LINQ Insertable Cardiac Monitor, LINQ II Insertable Cardiac Monitor, AccuRhythm AI ECG Classification System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K223630
510(k) Type
Traditional
Applicant
Medtronic, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/5/2023
Days to Decision
121 days
Submission Type
Summary