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FDA 510(k)

Cryopush Cold Compression Device

K-Number: K222669 · 2022-12-05

Decision Date2022-12-05
Product CodeIRP
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

Cryopush Cold Compression Device is a medical device manufactured by Chengdu Cryo-Push Medical Technology Co.,Ltd. It received FDA 510(k) clearance on 2022-12-05 under approval number K222669. 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?

Cryopush Cold Compression Device is a medical device that received FDA 510(k) clearance on 2022-12-05. It is manufactured by Chengdu Cryo-Push Medical Technology Co.,Ltd. The 510(k) number is K222669.

When was Cryopush Cold Compression Device approved by the FDA?

Cryopush Cold Compression Device received FDA 510(k) clearance on 2022-12-05, under approval number K222669.

What company makes Cryopush Cold Compression Device?

Cryopush Cold Compression Device is manufactured by Chengdu Cryo-Push Medical Technology Co.,Ltd.

What is the FDA product code for Cryopush Cold Compression Device?

The FDA product code for Cryopush Cold Compression Device is IRP.

Related Clinical Trials

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

Related Devices (Code: IRP)

Official Source

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