Cryopush Cold Compression Device
K-Number: K222669 · 2022-12-05
Device Summary
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. The listed applicant is Chengdu Cryo-Push Medical Technology Co.,Ltd. The 510(k) number is K222669.
When did Cryopush Cold Compression Device receive FDA 510(k) clearance?
Cryopush Cold Compression Device received FDA 510(k) clearance on 2022-12-05, under 510(k) number K222669.
Who is the listed applicant for Cryopush Cold Compression Device?
The FDA 510(k) record lists Chengdu Cryo-Push Medical Technology Co.,Ltd as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Cryopush Cold Compression Device?
The FDA product code for Cryopush Cold Compression Device is IRP.
Other records listing Chengdu Cryo-Push Medical Technology Co.,Ltd as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: IRP)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
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.