Rapid Reboot Recovery Products, LLC
FDA 510(k) & PMA Approved Devices — 2 products
Total Devices2
Categories1
Latest Approval2020-12-22
| Type | Number | Device Name | Code | Date | |
|---|---|---|---|---|---|
| 510(k) | K203552 | Rapid Reboot | IRP | 2020-12-22 | View |
| 510(k) | K182668 | Rapid Reboot Compression Therapy System | IRP | 2018-12-14 | View |
No matching devices.