Clearance Summary
SUNPEX TECHNOLOGIES MODEL SE 01 received FDA 510(k) clearance under submission number K021925, sponsored by Sunpex Technology Co., Ltd.. The device was reviewed via the Abbreviated premarket notification pathway and assigned to the Physical Medicine review panel. The statutory decision date of record is 2002-11-08.
- Submission: K021925
- Applicant / Sponsor: Sunpex Technology Co., Ltd.
- Clearance pathway: Abbreviated
- Review panel: Physical Medicine
- Device class: Class II
- Regulation citation: 21 CFR 890.3800
- Decision date: 2002-11-08
Classification & Regulation
This clearance is catalogued under FDA product code INI and 21 CFR 890.3800, within the Physical Medicine review panel as a Class II device.