Leg Massager (Models:RP-ALM070H, RP-ALM071H)— 510(k) K232965

Name: FDA 510(k) clearance K232965
Creator: U.S. Food and Drug Administration
Published: 2024-11-20

Substantially Equivalent

Shenzhen Ruiyi Business Technology Co., Ltd.

FDA 510(k) clearance K232965 for Leg Massager (Models:RP-ALM070H, RP-ALM071H), Substantially Equivalent on 2024-11-20. Applicant: Shenzhen Ruiyi Business Technology Co., Ltd.. Device class: 2.

Clearance details

Applicant: Shenzhen Ruiyi Business Technology Co., Ltd.
Product code: Code IRP
Device class: Class 2
Regulation: 21 CFR 890.5650
Advisory panel: Physical Medicine
Date received: 2023-09-21
Decision date: 2024-11-20
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Shenzhen, CN

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.