Clearance Summary
YOSHIDA RIDO-F, MODEL LM-01 received FDA 510(k) clearance under submission number K813348, sponsored by Kaycor Intl., Ltd.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 1982-01-07.
- Submission: K813348
- Applicant / Sponsor: Kaycor Intl., Ltd.
- Clearance pathway: Traditional
- Review panel: Dental
- Device class: Class I
- Regulation citation: 21 CFR 872.4200
- Decision date: 1982-01-07
Classification & Regulation
This clearance is catalogued under FDA product code EKX and 21 CFR 872.4200, within the Dental review panel as a Class I device.