# K212713: Air compression leg massager HY-1117A

- Pathway: 510(k) (Traditional)
- Applicant: Xiamen High Top Electronic Technology Co., Ltd.
- Decided: Jan 18, 2022 after 145 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: 9 generations back to K850316 (1985). 20 ancestors in all.
No later device cites it as a predicate yet.
0 of 21 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K193354: Air Compression Therapy Device, Shenzhen Dongjilian Electronics Co., Ltd. (2020) Summary page 5.

## Indications for use
Air compression leg massager HY-1117A is intended for home 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/K212713
Methodology: https://510kreport.com/methodology