Clearance Summary
GDC-1475 received FDA 510(k) clearance under submission number K904614, sponsored by Deringer-Ney, 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 1990-12-19.
- Submission: K904614
- Applicant / Sponsor: Deringer-Ney, Inc.
- Clearance pathway: Traditional
- Review panel: Dental
- Device class: Class II
- Regulation citation: 21 CFR 872.3060
- Decision date: 1990-12-19
Classification & Regulation
This clearance is catalogued under FDA product code EJT and 21 CFR 872.3060, within the Dental review panel as a Class II device.