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FDA 510(k)

Cryopush Cold Compression Device (A02-P-001)

K-Number: K253076 · 2026-04-02

Decision Date2026-04-02
Product CodeIRP
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

Cryopush Cold Compression Device (A02-P-001) is a medical device manufactured by Chengdu Cryo-Push Medical Technology Co.,Ltd. It received FDA 510(k) clearance on 2026-04-02 under approval number K253076. The device is classified under product code IRP. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Cryopush Cold Compression Device (A02-P-001)?

Cryopush Cold Compression Device (A02-P-001) is a medical device that received FDA 510(k) clearance on 2026-04-02. It is manufactured by Chengdu Cryo-Push Medical Technology Co.,Ltd. The 510(k) number is K253076.

When was Cryopush Cold Compression Device (A02-P-001) approved by the FDA?

Cryopush Cold Compression Device (A02-P-001) received FDA 510(k) clearance on 2026-04-02, under approval number K253076.

What company makes Cryopush Cold Compression Device (A02-P-001)?

Cryopush Cold Compression Device (A02-P-001) is manufactured by Chengdu Cryo-Push Medical Technology Co.,Ltd.

What is the FDA product code for Cryopush Cold Compression Device (A02-P-001)?

The FDA product code for Cryopush Cold Compression Device (A02-P-001) is IRP.

Related Clinical Trials

Other Devices by Chengdu Cryo-Push Medical Technology Co.,Ltd

Related Devices (Code: IRP)

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.