# K203552: Rapid Reboot

- Pathway: 510(k) (Traditional)
- Applicant: Rapid Reboot Recovery Products, LLC
- Decided: Dec 22, 2020 after 18 days
- Product code: IRP (Massager, Powered Inflatable Tube)
- Device class: 2
- Regulation: 21 CFR 890.5650
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 8 generations back to K850316 (1985). 19 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 21 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K182668: Rapid Reboot Compression Therapy System, Rapid Reboot Recovery Products, LLC (2018) Summary page 4.

## Most influential descendants
- K251622: Hand Massager (SM004D) (2026), 0 descendants of its own

## Indications for use
The Rapid Reboot REGEN+, REGEN, or GENESIS Compression Therapy Systems are indicated for the temporary relief of minor muscle aches and pains and for temporary increase in circulation to the treated areas in people who are in good the Rapid Reboot REGEN+, REGEN, or GENESIS Compression Therapy Systems simulate kneading and stroking of tissues by using an inflatable garment.

Source page: https://510kreport.com/device/K203552
Methodology: https://510kreport.com/methodology