Last synced on 18 April 2025 at 11:05 pm

OneTouch Ultra Plus Flex Blood Glucose Monitoring System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K151611
510(k) Type
Traditional
Applicant
LIFESCAN EUROPE
Country
Switzerland
FDA Decision
Substantially Equivalent
Decision Date
12/14/2015
Days to Decision
182 days
Submission Type
Summary

OneTouch Ultra Plus Flex Blood Glucose Monitoring System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K151611
510(k) Type
Traditional
Applicant
LIFESCAN EUROPE
Country
Switzerland
FDA Decision
Substantially Equivalent
Decision Date
12/14/2015
Days to Decision
182 days
Submission Type
Summary