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Study Watch with Irregular Pulse Monitor

Page Type
Cleared 510(K)
510(k) Number
K192415
510(k) Type
Traditional
Applicant
Verily Life Sciences LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/17/2020
Days to Decision
135 days
Submission Type
Summary

Study Watch with Irregular Pulse Monitor

Page Type
Cleared 510(K)
510(k) Number
K192415
510(k) Type
Traditional
Applicant
Verily Life Sciences LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/17/2020
Days to Decision
135 days
Submission Type
Summary