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Fitbit Irregular Rhythm Notifications

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K212372
510(k) Type
Traditional
Applicant
Fitbit, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/8/2022
Days to Decision
252 days
Submission Type
Summary

Fitbit Irregular Rhythm Notifications

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K212372
510(k) Type
Traditional
Applicant
Fitbit, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/8/2022
Days to Decision
252 days
Submission Type
Summary