Cryopush Cold Compression Device (A02-P-001)
K-Number: K253076 · 2026-04-02
Device Summary
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. The listed applicant is Chengdu Cryo-Push Medical Technology Co.,Ltd. The 510(k) number is K253076.
When did Cryopush Cold Compression Device (A02-P-001) receive FDA 510(k) clearance?
Cryopush Cold Compression Device (A02-P-001) received FDA 510(k) clearance on 2026-04-02, under 510(k) number K253076.
Who is the listed applicant for Cryopush Cold Compression Device (A02-P-001)?
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 (A02-P-001)?
The FDA product code for Cryopush Cold Compression Device (A02-P-001) 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.