Clearance Summary
EYE TRAY received FDA 510(k) clearance under submission number K912105, sponsored by Medical Device Inspection Co., Inc.. 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 1991-08-29.
- Submission: K912105
- Applicant / Sponsor: Medical Device Inspection Co., Inc.
- Clearance pathway: Traditional
- Review panel: General, Plastic Surgery
- Device class: Class I
- Regulation citation: 21 CFR 878.4800
- Decision date: 1991-08-29
Classification & Regulation
This clearance is catalogued under FDA product code LRP and 21 CFR 878.4800, within the General, Plastic Surgery review panel as a Class I device.