Clearance Summary
AXENIC DHP DISPOSABLE HIGH-PERFORMANCE HANDPIECE received FDA 510(k) clearance under submission number K072754, sponsored by Axenic Dental, 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 2008-01-25.
- Submission: K072754
- Applicant / Sponsor: Axenic Dental, Inc.
- Clearance pathway: Traditional
- Review panel: Dental
- Device class: Class I
- Regulation citation: 21 CFR 872.4200
- Decision date: 2008-01-25
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.