Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

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 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.

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. 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.

Other records listing Shenzhen Ruiyi Business Technology Co., Ltd. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K222924Leg Massager RF-ALM070

Related Devices (Code: IRP)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K260944ManaCold Compression SystemManamed, LLCK260529Air Compression Massager (HY-1165)Xiamen High Top Electronic Technology Co., Ltd.K260948Air Compression Massager (EP30B001 I)Wavepulse (Xiamen) Healthcare Technology Co., Ltd.K253919Cryo And Thermo Therapy SystemXiamen Weiyou Intelligent Technology Co., Ltd.K252396Cryo Sport 2.0 (AVA 501)Avanutri Equipamentos DE SaúdeK254200Air Compression Leg Massager (LF-FT001, LF-FT002-1, LF-FT003, LF-FT003-1, LF-FT004-1, LF-FT005-1, LF-FT006-1, LF-FT007, LF-FT008, LF-FT009, LF-FT010, LF-FT011, LF-FT012, LF-FT013, LF-FT014, LF-FT015, LF-FT016, UM-01, UM-02, UM-03, UM-03-1, UM-04-1, UM-05-1, UM-06-1, UM-07, UM-08, UM-09, UM-10, UM-11, UM-12, UM-13, UM-14, UM-15, UM-16, AI-01, AI-02, AI-03, AI-04, AI-05, AI-06, AI01, AI02, AI03, AI-07, AI-08, AI-09, AI-10, AI-11, AI-12, AI-13, AI-14)Wenzhou Lingfeng Electronic Technology Co., Ltd.

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.

↑