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LINQ II Insertable Cardiac Monitor

Page Type
Cleared 510(K)
510(k) Number
K221962
510(k) Type
Traditional
Applicant
Medtronic, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/25/2022
Days to Decision
51 days
Submission Type
Summary

LINQ II Insertable Cardiac Monitor

Page Type
Cleared 510(K)
510(k) Number
K221962
510(k) Type
Traditional
Applicant
Medtronic, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/25/2022
Days to Decision
51 days
Submission Type
Summary