Cold Compression Wrap Pro
K-Number: K230524 · 2024-01-19
Decision Date2024-01-19
Product CodeIRP
Advisory CommitteePM
DecisionSubstantially Equivalent
Device Summary
Cold Compression Wrap Pro is a medical device manufactured by Chengdu Cryo-Push Medical Technology Co.,Ltd. It received FDA 510(k) clearance on 2024-01-19 under approval number K230524. 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 Cold Compression Wrap Pro?
Cold Compression Wrap Pro is a medical device that received FDA 510(k) clearance on 2024-01-19. It is manufactured by Chengdu Cryo-Push Medical Technology Co.,Ltd. The 510(k) number is K230524.
When was Cold Compression Wrap Pro approved by the FDA?
Cold Compression Wrap Pro received FDA 510(k) clearance on 2024-01-19, under approval number K230524.
What company makes Cold Compression Wrap Pro?
Cold Compression Wrap Pro is manufactured by Chengdu Cryo-Push Medical Technology Co.,Ltd.
What is the FDA product code for Cold Compression Wrap Pro?
The FDA product code for Cold Compression Wrap Pro 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.