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FDA 510(k)

Air Compression Leg Massager (Model: LY-670D)

K-Number: K222949 · 2022-12-22

ApplicantZhejiang Luyao Electronics Technology Co., Ltd.
Decision Date2022-12-22
Product CodeIRP
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

Air Compression Leg Massager (Model: LY-670D) is a medical device manufactured by Zhejiang Luyao Electronics Technology Co., Ltd.. It received FDA 510(k) clearance on 2022-12-22 under approval number K222949. 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 Air Compression Leg Massager (Model: LY-670D)?

Air Compression Leg Massager (Model: LY-670D) is a medical device that received FDA 510(k) clearance on 2022-12-22. It is manufactured by Zhejiang Luyao Electronics Technology Co., Ltd.. The 510(k) number is K222949.

When was Air Compression Leg Massager (Model: LY-670D) approved by the FDA?

Air Compression Leg Massager (Model: LY-670D) received FDA 510(k) clearance on 2022-12-22, under approval number K222949.

What company makes Air Compression Leg Massager (Model: LY-670D)?

Air Compression Leg Massager (Model: LY-670D) is manufactured by Zhejiang Luyao Electronics Technology Co., Ltd..

What is the FDA product code for Air Compression Leg Massager (Model: LY-670D)?

The FDA product code for Air Compression Leg Massager (Model: LY-670D) 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.

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