Last synced on 30 May 2025 at 11:05 pm

LINQ II Insertable Cardiac Monitor, Zelda 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
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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