K243206
- 510(k) number
- K243206
- Device name
- Air compression massager (ACM-PLUS-A1, ACM-PLUS-A2, ACM-PLUS-A3, ACM-PLUS-A4, ACM-PLUS-A5, ACM-PLUS-A6)
- Applicant
- Sichuan Qianli-Beoka Medical Technology, Inc. CN
- Product code
- IRP — Massager, Powered Inflatable Tube
- Decision date
- 2025-02-19
- Date received
- 2024-10-01
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Physical Medicine
PDFDownload 510(k) SummaryArchived here · 0.7 MB · U.S. public domain
Also available from FDA: K243206.pdf
Official FDA record: K243206
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.