Cold Compression
K-Number: K240986 · 2024-05-01
ApplicantJkh Health Co., Ltd.
Decision Date2024-05-01
Product CodeIRP
Advisory CommitteePM
DecisionSubstantially Equivalent
Device Summary
Cold Compression is a medical device manufactured by Jkh Health Co., Ltd.. It received FDA 510(k) clearance on 2024-05-01 under approval number K240986. 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?
Cold Compression is a medical device that received FDA 510(k) clearance on 2024-05-01. It is manufactured by Jkh Health Co., Ltd.. The 510(k) number is K240986.
When was Cold Compression approved by the FDA?
Cold Compression received FDA 510(k) clearance on 2024-05-01, under approval number K240986.
What company makes Cold Compression?
Cold Compression is manufactured by Jkh Health Co., Ltd..
What is the FDA product code for Cold Compression?
The FDA product code for Cold Compression is IRP.
Other Devices by Jkh Health Co., Ltd.
K153520Electronic Pulse Stimulator
K162517Electronic Pulse Stimulator Model: PL-029K12 and PL-029K13
K200561StimPlus Patch, StimPlus Patch, StimPlus Patch
K202839Overlapped Compression Therapy
K211050Infrared Thermometer, Model: JKH-300, JKH-301, JKH-302, JKH-303, JKH-304
K223541Cold/Hot Compression
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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.