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Study Watch with Irregular Pulse Monitor (Home), Study Watch with Irregular Pulse Monitor

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K213357
510(k) Type
Traditional
Applicant
Verily Life Sciences LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/19/2022
Days to Decision
280 days
Submission Type
Summary

Study Watch with Irregular Pulse Monitor (Home), Study Watch with Irregular Pulse Monitor

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K213357
510(k) Type
Traditional
Applicant
Verily Life Sciences LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/19/2022
Days to Decision
280 days
Submission Type
Summary