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FDA 510(k)

Leg Massager (Models:RP-ALM070H, RP-ALM071H)

K-Number: K232965 · 2024-11-20

ApplicantShenzhen Ruiyi Business Technology Co., Ltd.
Decision Date2024-11-20
Product CodeIRP
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

Leg Massager (Models:RP-ALM070H, RP-ALM071H) is a medical device manufactured by Shenzhen Ruiyi Business Technology Co., Ltd.. It received FDA 510(k) clearance on 2024-11-20 under approval number K232965. 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 Leg Massager (Models:RP-ALM070H, RP-ALM071H)?

Leg Massager (Models:RP-ALM070H, RP-ALM071H) is a medical device that received FDA 510(k) clearance on 2024-11-20. It is manufactured by Shenzhen Ruiyi Business Technology Co., Ltd.. The 510(k) number is K232965.

When was Leg Massager (Models:RP-ALM070H, RP-ALM071H) approved by the FDA?

Leg Massager (Models:RP-ALM070H, RP-ALM071H) received FDA 510(k) clearance on 2024-11-20, under approval number K232965.

What company makes Leg Massager (Models:RP-ALM070H, RP-ALM071H)?

Leg Massager (Models:RP-ALM070H, RP-ALM071H) is manufactured by Shenzhen Ruiyi Business Technology Co., Ltd..

What is the FDA product code for Leg Massager (Models:RP-ALM070H, RP-ALM071H)?

The FDA product code for Leg Massager (Models:RP-ALM070H, RP-ALM071H) is IRP.

Other Devices by Shenzhen Ruiyi Business Technology Co., Ltd.

K222924Leg Massager RF-ALM070

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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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