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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