FDA 510(k) Applications Submitted by Rapid Reboot Recovery Products, LLC
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K182668 | 09/25/2018 | Rapid Reboot Compression Therapy System | Rapid Reboot Recovery Products, LLC |
| K203552 | 12/04/2020 | Rapid Reboot | Rapid Reboot Recovery Products, LLC |
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