Clearance Summary
KAVO INTRASEPT 905 received FDA 510(k) clearance under submission number K934783, sponsored by Kavo America. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 1994-05-16.
- Submission: K934783
- Applicant / Sponsor: Kavo America
- Clearance pathway: Traditional
- Review panel: Dental
- Device class: Class I
- Regulation citation: 21 CFR 872.6640
- Decision date: 1994-05-16
Classification & Regulation
This clearance is catalogued under FDA product code EIA and 21 CFR 872.6640, within the Dental review panel as a Class I device.