Clearance Summary
ATHENA HIGH SPEED HANDPIECE received FDA 510(k) clearance under submission number K925678, sponsored by Athena Technology, 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 1994-12-15.
- Submission: K925678
- Applicant / Sponsor: Athena Technology, Inc.
- Clearance pathway: Traditional
- Review panel: Dental
- Device class: Class I
- Regulation citation: 21 CFR 872.4200
- Decision date: 1994-12-15
Classification & Regulation
This clearance is catalogued under FDA product code EFB and 21 CFR 872.4200, within the Dental review panel as a Class I device.