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. 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.
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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.