Clearance Summary
OMNILIGHT FLUORESCENT PULSED LIGHT SYSTEM received FDA 510(k) clearance under submission number K032191, sponsored by Luxsano AB. The device was reviewed via the Special premarket notification pathway and assigned to the General, Plastic Surgery review panel. The statutory decision date of record is 2003-08-20.
- Submission: K032191
- Applicant / Sponsor: Luxsano AB
- Clearance pathway: Special
- Review panel: General, Plastic Surgery
- Device class: Class II
- Regulation citation: 21 CFR 878.4810
- Decision date: 2003-08-20
Classification & Regulation
This clearance is catalogued under FDA product code GEX and 21 CFR 878.4810, within the General, Plastic Surgery review panel as a Class II device.