FDA 510(k)

腿部按摩器（型号：RP-ALM070H, RP-ALM071H）

K号: K232965 · 2024-11-20

申请人Shenzhen Ruiyi Business Technology Co., Ltd.

决定日期2024-11-20

产品代码IRP

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决定实质等同

器械摘要

Leg Massager (Models:RP-ALM070H, RP-ALM071H) is the device name listed in this FDA 510(k) record. The listed applicant is Shenzhen Ruiyi Business Technology Co., Ltd.. It received FDA 510(k) clearance on 2024-11-20 under 510(k) number K232965. The device is classified under product code IRP. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

常见问题

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. The listed applicant is Shenzhen Ruiyi Business Technology Co., Ltd.. The 510(k) number is K232965.

When did Leg Massager (Models:RP-ALM070H, RP-ALM071H) receive FDA 510(k) clearance?

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

Who is the listed applicant for Leg Massager (Models:RP-ALM070H, RP-ALM071H)?

The FDA 510(k) record lists Shenzhen Ruiyi Business Technology Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

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.

列明Shenzhen Ruiyi Business Technology Co., Ltd.为申报人的其他记录

关联记录通过名称、产品代码或其他元数据自动匹配。匹配不意味着已验证临床、科学、企业或监管关系；请查阅链接的官方来源。

K222924腿部按摩器 RF-ALM070

相关器械（代码：IRP）

关联记录通过名称、产品代码或其他元数据自动匹配。匹配不意味着已验证临床、科学、企业或监管关系；请查阅链接的官方来源。

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官方来源

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