Clearance Summary
LIGHTLAS FAMILY OF MULTI-WAVELENGTH MEDICAL LASER SYSTEM received FDA 510(k) clearance under submission number K124043, sponsored by Lightmed Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Ophthalmic review panel. The statutory decision date of record is 2013-09-26.
- Submission: K124043
- Applicant / Sponsor: Lightmed Corp.
- Clearance pathway: Traditional
- Review panel: Ophthalmic
- Device class: Class II
- Regulation citation: 21 CFR 886.4390
- Decision date: 2013-09-26
Classification & Regulation
This clearance is catalogued under FDA product code HQF and 21 CFR 886.4390, within the Ophthalmic review panel as a Class II device.