Clearance Summary
LUCENTLITE, MODEL IMD 010 received FDA 510(k) clearance under submission number K033072, sponsored by Industrial & Medical Design, 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 2004-04-01.
- Submission: K033072
- Applicant / Sponsor: Industrial & Medical Design, Inc.
- Clearance pathway: Traditional
- Review panel: General, Plastic Surgery
- Device class: Class II
- Regulation citation: 21 CFR 878.4810
- Decision date: 2004-04-01
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.