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LINQ II Insertable Cardiac Monitor, Zelda AI ECG Classification System

Page Type
Cleared 510(K)
510(k) Number
K210484
510(k) Type
Traditional
Applicant
Medtronic, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/11/2021
Days to Decision
112 days
Submission Type
Summary

LINQ II Insertable Cardiac Monitor, Zelda AI ECG Classification System

Page Type
Cleared 510(K)
510(k) Number
K210484
510(k) Type
Traditional
Applicant
Medtronic, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/11/2021
Days to Decision
112 days
Submission Type
Summary