Cold Compression
K-Number: K240986 · 2024-05-01
Device Summary
Frequently Asked Questions
What is the Cold Compression?
Cold Compression is a medical device that received FDA 510(k) clearance on 2024-05-01. The listed applicant is Jkh Health Co., Ltd.. The 510(k) number is K240986.
When did Cold Compression receive FDA 510(k) clearance?
Cold Compression received FDA 510(k) clearance on 2024-05-01, under 510(k) number K240986.
Who is the listed applicant for Cold Compression?
The FDA 510(k) record lists Jkh Health Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Cold Compression?
The FDA product code for Cold Compression is IRP.
Related Clinical Trials
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.
Other records listing Jkh Health 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.