FDA 510(k) Applications Submitted by Xtreem Pulse, LLC
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K173483 | 11/13/2017 | Pure Flow External Counter-Pulsation Device | Xtreem Pulse, LLC |
| K190269 | 02/08/2019 | PureLift | Xtreem Pulse, LLC |
Search | Companies | Product Codes | Device Names | Contacts | Applications | Decisions | Contact