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FDA 510(k)

Rapid Reboot

K-Number: K203552 · 2020-12-22

ApplicantRapid Reboot Recovery Products, LLC
Decision Date2020-12-22
Product CodeIRP
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

Rapid Reboot is a medical device manufactured by Rapid Reboot Recovery Products, LLC. It received FDA 510(k) clearance on 2020-12-22 under approval number K203552. The device is classified under product code IRP. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Rapid Reboot?

Rapid Reboot is a medical device that received FDA 510(k) clearance on 2020-12-22. It is manufactured by Rapid Reboot Recovery Products, LLC. The 510(k) number is K203552.

When was Rapid Reboot approved by the FDA?

Rapid Reboot received FDA 510(k) clearance on 2020-12-22, under approval number K203552.

What company makes Rapid Reboot?

Rapid Reboot is manufactured by Rapid Reboot Recovery Products, LLC.

What is the FDA product code for Rapid Reboot?

The FDA product code for Rapid Reboot is IRP.

Other Devices by Rapid Reboot Recovery Products, LLC

K182668Rapid Reboot Compression Therapy System

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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