Clearance Summary
RX 91 received FDA 510(k) clearance under submission number K823100, sponsored by Bauer, Cheng & Associates, 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 1982-11-10.
- Submission: K823100
- Applicant / Sponsor: Bauer, Cheng & Associates, Inc.
- Clearance pathway: Traditional
- Review panel: Dental
- Device class: Class II
- Regulation citation: 21 CFR 872.3060
- Decision date: 1982-11-10
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.