K232965
- 510(k) number
- K232965
- Device name
- Leg Massager (Models:RP-ALM070H, RP-ALM071H)
- Applicant
- Shenzhen Ruiyi Business Technology Co., Ltd. CN
- Product code
- IRP — Massager, Powered Inflatable Tube
- Decision date
- 2024-11-20
- Date received
- 2023-09-21
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Physical Medicine
PDFDownload 510(k) SummaryArchived here · 0.5 MB · U.S. public domain
Also available from FDA: K232965.pdf
Official FDA record: K232965
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.