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FDA 510(k) Applications Submitted by NIKI SKELLY
FDA 510(k) Number
Submission Date
Device Name
Applicant
K151611
06/15/2015
OneTouch Ultra Plus Flex Blood Glucose Monitoring System
LIFESCAN EUROPE
K193475
12/16/2019
OneTouch Verio Reflect Blood Glucose Monitoring System
LifeScan Europe GmbH
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