Clearance Summary
MICROLIGHT 830 LASER SYSTEM received FDA 510(k) clearance under submission number K010175, sponsored by Microlight Corporation of America. 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 2002-02-06.
- Submission: K010175
- Applicant / Sponsor: Microlight Corporation of America
- Clearance pathway: Traditional
- Review panel: Physical Medicine
- Device class: Class II
- Regulation citation: 21 CFR 890.5500
- Decision date: 2002-02-06
Classification & Regulation
This clearance is catalogued under FDA product code NHN and 21 CFR 890.5500, within the Physical Medicine review panel as a Class II device.