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FDA 510(k) Applications Submitted by LIFESCAN EUROPE
FDA 510(k) Number
Submission Date
Device Name
Applicant
K150214
01/30/2015
OneTouch Verio Flex Blood Glucose Monitoring System
LIFESCAN EUROPE
K151611
06/15/2015
OneTouch Ultra Plus Flex Blood Glucose Monitoring System
LIFESCAN EUROPE
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