K242140
- 510(k) number
- K242140
- Device name
- Air Compression Leg Massager (K-705)
- Applicant
- Jiale Health Technology Shenzhen Co., Ltd. CN
- Product code
- IRP — Massager, Powered Inflatable Tube
- Decision date
- 2025-03-17
- Date received
- 2024-07-22
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Physical Medicine
PDFDownload 510(k) SummaryArchived here · 0.8 MB · U.S. public domain
Also available from FDA: K242140.pdf
Official FDA record: K242140
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.