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Zio AT® device (A100A1001)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K240029
510(k) Type
Traditional
Applicant
iRhythm Technologies, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/21/2024
Days to Decision
291 days
Submission Type
Summary

Zio AT® device (A100A1001)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K240029
510(k) Type
Traditional
Applicant
iRhythm Technologies, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/21/2024
Days to Decision
291 days
Submission Type
Summary