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FDA 510(k)

YY-A02-B Overlapped Compression Therapy

K-Number: K221862 · 2022-12-08

ApplicantHuizhou Xinyi Technology Co., Ltd.
Decision Date2022-12-08
Product CodeIRP
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

YY-A02-B Overlapped Compression Therapy is a medical device manufactured by Huizhou Xinyi Technology Co., Ltd.. It received FDA 510(k) clearance on 2022-12-08 under approval number K221862. 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 YY-A02-B Overlapped Compression Therapy?

YY-A02-B Overlapped Compression Therapy is a medical device that received FDA 510(k) clearance on 2022-12-08. It is manufactured by Huizhou Xinyi Technology Co., Ltd.. The 510(k) number is K221862.

When was YY-A02-B Overlapped Compression Therapy approved by the FDA?

YY-A02-B Overlapped Compression Therapy received FDA 510(k) clearance on 2022-12-08, under approval number K221862.

What company makes YY-A02-B Overlapped Compression Therapy?

YY-A02-B Overlapped Compression Therapy is manufactured by Huizhou Xinyi Technology Co., Ltd..

What is the FDA product code for YY-A02-B Overlapped Compression Therapy?

The FDA product code for YY-A02-B Overlapped Compression Therapy is IRP.

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 Huizhou Xinyi Technology Co., Ltd.

K240981Air compression leg massager

Related Devices (Code: IRP)

K160608NormaTec Pulse and NormaTec Pulse ProNormaTec Industries, LP K171685Med4 EliteCool Systems, Inc. (Dba Game Ready) K161907Pressure Therapy SystemXiamen Senyang Co., Ltd. K163280RP Lite 760RMego Afek AC , Ltd. K160178Lympha-Flow(LF1200)Daesung Maref Co., Ltd. K183169Pulse 2.0, Pulse Pro 2.0NormaTec Industries, LP

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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