Clearance Summary
FLOOR LIGHT received FDA 510(k) clearance under submission number K882333, sponsored by Commercial Products & Engineering Co.. The device was reviewed via the Traditional premarket notification pathway and assigned to the General, Plastic Surgery review panel. The statutory decision date of record is 1988-06-23.
- Submission: K882333
- Applicant / Sponsor: Commercial Products & Engineering Co.
- Clearance pathway: Traditional
- Review panel: General, Plastic Surgery
- Device class: Class II
- Regulation citation: 21 CFR 878.4580
- Decision date: 1988-06-23
Classification & Regulation
This clearance is catalogued under FDA product code FSS and 21 CFR 878.4580, within the General, Plastic Surgery review panel as a Class II device.