Rapid Reboot Recovery Products, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Rapid Reboot Recovery Products, LLC - FDA 510(k) Cleared Devices
Recent clearances: Rapid Reboot, Rapid Reboot Compression Therapy System
2
Total
2
Cleared
0
Denied
Rapid Reboot Recovery Products, LLC has 2 FDA 510(k) cleared medical devices. Based in Lindon, US.
Historical record: 2 cleared submissions from 2018 to 2020. Primary specialty: Physical Medicine.
Browse the FDA 510(k) cleared devices submitted by Rapid Reboot Recovery Products, LLC Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by FDA Consulting, LLC and Regulatory Technology Services, LLC.
FDA 510(k) Regulatory Record - Rapid Reboot Recovery Products, LLC
2 devices