Clearance Summary
AGATHA-A-H2010 received FDA 510(k) clearance under submission number K983374, sponsored by Midian Intl.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 1998-12-23.
- Submission: K983374
- Applicant / Sponsor: Midian Intl.
- Clearance pathway: Traditional
- Review panel: Dental
- Device class: Class I
- Regulation citation: 21 CFR 872.6510
- Decision date: 1998-12-23
Classification & Regulation
This clearance is catalogued under FDA product code EFS and 21 CFR 872.6510, within the Dental review panel as a Class I device.