Clearance Summary
ARISTOSURG 250 received FDA 510(k) clearance under submission number K800395, sponsored by Halmon-Locren, 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 1980-03-17.
- Submission: K800395
- Applicant / Sponsor: Halmon-Locren, Inc.
- Clearance pathway: Traditional
- Review panel: Dental
- Device class: Class I
- Regulation citation: 21 CFR 872.6640
- Decision date: 1980-03-17
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.