Clearance Summary
MONOGRAM II received FDA 510(k) clearance under submission number K895064, sponsored by Leach and Dillon Co., 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 1989-12-18.
- Submission: K895064
- Applicant / Sponsor: Leach and Dillon Co., Inc.
- Clearance pathway: Traditional
- Review panel: Dental
- Device class: Class II
- Regulation citation: 21 CFR 872.3060
- Decision date: 1989-12-18
Classification & Regulation
This clearance is catalogued under FDA product code EJT and 21 CFR 872.3060, within the Dental review panel as a Class II device.