Clearance Summary
PRELUDE received FDA 510(k) clearance under submission number K040952, sponsored by Danville Materials, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2004-06-29.
- Submission: K040952
- Applicant / Sponsor: Danville Materials, Inc.
- Clearance pathway: Traditional
- Review panel: Dental
- Device class: Class II
- Regulation citation: 21 CFR 872.3200
- Decision date: 2004-06-29
Classification & Regulation
This clearance is catalogued under FDA product code KLE and 21 CFR 872.3200, within the Dental review panel as a Class II device.