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FDA 510(k)

Overlapped Compression Therapy

K-Number: K202839 · 2021-01-21

ApplicantJkh Health Co., Ltd.
Decision Date2021-01-21
Product CodeJOW
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

Overlapped Compression Therapy is a medical device manufactured by Jkh Health Co., Ltd.. It received FDA 510(k) clearance on 2021-01-21 under approval number K202839. The device is classified under product code JOW. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Overlapped Compression Therapy?

Overlapped Compression Therapy is a medical device that received FDA 510(k) clearance on 2021-01-21. It is manufactured by Jkh Health Co., Ltd.. The 510(k) number is K202839.

When was Overlapped Compression Therapy approved by the FDA?

Overlapped Compression Therapy received FDA 510(k) clearance on 2021-01-21, under approval number K202839.

What company makes Overlapped Compression Therapy?

Overlapped Compression Therapy is manufactured by Jkh Health Co., Ltd..

What is the FDA product code for Overlapped Compression Therapy?

The FDA product code for Overlapped Compression Therapy is JOW.

Related Clinical Trials

NCT07600489 A Randomized Non-Inferiority Study of Mepi™ Press 2 vs UrgoK2® for Compression Therapy in Venous Leg Ulcers NOT_YET_RECRUITING NCT06911385 Augmenting Cerebral Blood Flow in Acute Ischemic Stroke NOT_YET_RECRUITING NCT06545812 Immune Response During the Conservative and Minimal Invasive Treatment of Pain Caused by Lumbar Disc Herniation COMPLETED NCT07123285 Effect of Photobiomodulation on Healing of Venous Leg Ulcers NOT_YET_RECRUITING NCT07549594 Prophylaxis of Recurrent Erysipelas in Lower Limbs: compreSsion thErapy vs aNTibiotics and Compression Therapy. NOT_YET_RECRUITING NCT07550569 Effectiveness of High Intensity Laser Therapy in Management of Lumbar Disc Herniation NOT_YET_RECRUITING

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 K211050Infrared Thermometer, Model: JKH-300, JKH-301, JKH-302, JKH-303, JKH-304 K223541Cold/Hot Compression K240986Cold Compression

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Related Devices (Code: JOW)

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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.

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