Clearance Summary
DENAR ACCUCEPH CEPHALOMETER IMAGING SYSTEM received FDA 510(k) clearance under submission number K944162, sponsored by Teledyne Water Pik. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 1994-11-29.
- Submission: K944162
- Applicant / Sponsor: Teledyne Water Pik
- Clearance pathway: Traditional
- Review panel: Dental
- Device class: Class II
- Regulation citation: 21 CFR 872.1830
- Decision date: 1994-11-29
Classification & Regulation
This clearance is catalogued under FDA product code EAG and 21 CFR 872.1830, within the Dental review panel as a Class II device.