# K222669: Cryopush Cold Compression Device

- Pathway: 510(k) (Traditional)
- Applicant: Chengdu Cryo-Push Medical Technology Co.,Ltd
- Decided: Dec 5, 2022 after 90 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.
2 later devices descend from it; 2 cite it directly.
0 of 23 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 4.

## Most influential descendants
- K253076: Cryopush Cold Compression Device (A02-P-001) (2026), 0 descendants of its own
- K230524: Cold Compression Wrap Pro (2024), 0 descendants of its own

## Indications for use
A02-P-001: The Cryopush Cold Compression Device is indicated for the temporary relief of minor muscle aches and pains. The device is indicated for temporary increase in circulation of the treated areas in people who are in good health, and simulates kneading and stroking of tissues using by an inflatable wrap. The cold pack is indicated for localized therapy in situations where cold temperature therapy is necessary or desirable. A02-P-002: The Cryopush A02-P-002 is indicated for the temporary relief of minor muscle aches and pains. The device is indicated for temporary increase in circulation of the treated areas in people who are in good health, and simulates kneading and stroking of tissues using by an inflatable wrap.

Source page: https://510kreport.com/device/K222669
Methodology: https://510kreport.com/methodology