K240981
- 510(k) number
- K240981
- Device name
- Air compression leg massager
- Applicant
- Huizhou Xinyi Technology Co., Ltd. CN
- Product code
- IRP — Massager, Powered Inflatable Tube
- Decision date
- 2024-08-02
- Date received
- 2024-04-10
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Physical Medicine
This submission filed a 510(k) Statement rather than a Summary; no public summary is available from FDA.
Official FDA record: K240981
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.