Clearance Summary
Leg and Foot Air Wave Pressure Therapy Device received FDA 510(k) clearance under submission number K223464, sponsored by Zhangzhou Easepal Innovation CO , Ltd.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Physical Medicine review panel. The statutory decision date of record is 2023-03-14.
- Submission: K223464
- Applicant / Sponsor: Zhangzhou Easepal Innovation CO , Ltd.
- Clearance pathway: Traditional
- Review panel: Physical Medicine
- Device class: Class II
- Regulation citation: 21 CFR 890.5650
- Decision date: 2023-03-14
Classification & Regulation
This clearance is catalogued under FDA product code IRP and 21 CFR 890.5650, within the Physical Medicine review panel as a Class II device.