FDA 510(k) Applications Submitted by Andrew Barile
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K230506 | 02/24/2023 | PureLift Pro Edition | Xtreem Pulse |
| K221443 | 05/18/2022 | PureLift Pro Plus | Xtreem Pulse LLC |
| K173483 | 11/13/2017 | Pure Flow External Counter-Pulsation Device | Xtreem Pulse, LLC |
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