Clearance Summary
RITTER MODEL J DENTAL CHAIR received FDA 510(k) clearance under submission number K800084, sponsored by Ritter Co.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 1980-01-29.
- Submission: K800084
- Applicant / Sponsor: Ritter Co.
- Clearance pathway: Traditional
- Review panel: Dental
- Device class: Class I
- Regulation citation: 21 CFR 872.6250
- Decision date: 1980-01-29
Classification & Regulation
This clearance is catalogued under FDA product code KLC and 21 CFR 872.6250, within the Dental review panel as a Class I device.