K241446
- 510(k) number
- K241446
- Device name
- Air Compression Massager (ACM-A1, ACM-A2, ACM-A3, ACM-A4)
- Applicant
- Sichuan Qianii-Beoka Medical Technoiogy Lnc. CN
- Product code
- IRP — Massager, Powered Inflatable Tube
- Decision date
- 2024-10-08
- Date received
- 2024-05-22
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Physical Medicine
510(k) Summary (official FDA PDF): K241446.pdf
Official FDA record: K241446
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.