# K253076: Cryopush Cold Compression Device (A02-P-001)

- Pathway: 510(k) (Traditional)
- Applicant: Chengdu Cryo-Push Medical Technology Co.,Ltd
- Decided: Apr 2, 2026 after 191 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: 10 generations back to K850316 (1985). 21 ancestors in all.
No later device cites it as a predicate yet.
0 of 22 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K222669: Cryopush Cold Compression Device, Chengdu Cryo-Push Medical Technology Co.,Ltd (2022) Summary page 5.

## Indications for use
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.

Source page: https://510kreport.com/device/K253076
Methodology: https://510kreport.com/methodology