Clearance Summary
DENTURE RESIN received FDA 510(k) clearance under submission number K890830, sponsored by G-C Intl. Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 1989-05-01.
- Submission: K890830
- Applicant / Sponsor: G-C Intl. Corp.
- Clearance pathway: Traditional
- Review panel: Dental
- Device class: Class II
- Regulation citation: 21 CFR 872.3760
- Decision date: 1989-05-01
Classification & Regulation
This clearance is catalogued under FDA product code EBI and 21 CFR 872.3760, within the Dental review panel as a Class II device.