Leg Massager RF-ALM070
K-Number: K222924 · 2022-12-23
Decision Date2022-12-23
Product CodeIRP
Advisory CommitteePM
DecisionSubstantially Equivalent
Device Summary
Leg Massager RF-ALM070 is a medical device manufactured by Shenzhen Ruiyi Business Technology Co., Ltd.. It received FDA 510(k) clearance on 2022-12-23 under approval number K222924. 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 RF-ALM070?
Leg Massager RF-ALM070 is a medical device that received FDA 510(k) clearance on 2022-12-23. It is manufactured by Shenzhen Ruiyi Business Technology Co., Ltd.. The 510(k) number is K222924.
When was Leg Massager RF-ALM070 approved by the FDA?
Leg Massager RF-ALM070 received FDA 510(k) clearance on 2022-12-23, under approval number K222924.
What company makes Leg Massager RF-ALM070?
Leg Massager RF-ALM070 is manufactured by Shenzhen Ruiyi Business Technology Co., Ltd..
What is the FDA product code for Leg Massager RF-ALM070?
The FDA product code for Leg Massager RF-ALM070 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.