# K260529: Air Compression Massager (HY-1165)

- Pathway: 510(k) (Traditional)
- Applicant: Xiamen High Top Electronic Technology Co., Ltd.
- Decided: Jul 27, 2026 after 160 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: 11 generations back to K850316 (1985). 24 ancestors in all.
No later device cites it as a predicate yet.
0 of 25 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 6.
- K221666: Normatec Go, NormaTec Industries, LP (2022) Summary page 6.

## Indications for use
The air compression massager is an air pressure massager intended to temporarily relieve minor muscle aches and/or pains, and to temporarily increase circulation to the treated areas in people who are in good health.

Source page: https://510kreport.com/device/K260529
Methodology: https://510kreport.com/methodology