Clearance Summary
ARGEBOND 77+ received FDA 510(k) clearance under submission number K915165, sponsored by Argen Precious Metals, 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 1992-04-21.
- Submission: K915165
- Applicant / Sponsor: Argen Precious Metals, Inc.
- Clearance pathway: Traditional
- Review panel: Dental
- Device class: Class II
- Regulation citation: 21 CFR 872.3060
- Decision date: 1992-04-21
Classification & Regulation
This clearance is catalogued under FDA product code EJS and 21 CFR 872.3060, within the Dental review panel as a Class II device.