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LINQ II Insertable Cardiac Monitor

Page Type
Cleared 510(K)
510(k) Number
K233562
510(k) Type
Special
Applicant
Medtronic, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/6/2023
Days to Decision
30 days
Submission Type
Summary

LINQ II Insertable Cardiac Monitor

Page Type
Cleared 510(K)
510(k) Number
K233562
510(k) Type
Special
Applicant
Medtronic, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/6/2023
Days to Decision
30 days
Submission Type
Summary