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OneTouch Verio Reflect Blood Glucose Monitoring System

Page Type
Cleared 510(K)
510(k) Number
K193475
510(k) Type
Traditional
Applicant
LifeScan Europe GmbH
Country
Switzerland
FDA Decision
Substantially Equivalent
Decision Date
2/14/2020
Days to Decision
60 days
Submission Type
Summary

OneTouch Verio Reflect Blood Glucose Monitoring System

Page Type
Cleared 510(K)
510(k) Number
K193475
510(k) Type
Traditional
Applicant
LifeScan Europe GmbH
Country
Switzerland
FDA Decision
Substantially Equivalent
Decision Date
2/14/2020
Days to Decision
60 days
Submission Type
Summary