Clearance Summary
MODEL LA-1200 MULTI-CHANNEL LASER THERAPY SYSTEM received FDA 510(k) clearance under submission number K102134, sponsored by United Integrated Services 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 2010-12-23.
- Submission: K102134
- Applicant / Sponsor: United Integrated Services Co., Ltd.
- Clearance pathway: Traditional
- Review panel: Physical Medicine
- Device class: Class II
- Regulation citation: 21 CFR 890.5500
- Decision date: 2010-12-23
Classification & Regulation
This clearance is catalogued under FDA product code ILY and 21 CFR 890.5500, within the Physical Medicine review panel as a Class II device.