Clearance Summary
VISIO-BAND received FDA 510(k) clearance under submission number K810265, sponsored by Espe-Premier Sales 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 1981-02-23.
- Submission: K810265
- Applicant / Sponsor: Espe-Premier Sales Co.
- Clearance pathway: Traditional
- Review panel: Dental
- Device class: Class II
- Regulation citation: 21 CFR 872.3200
- Decision date: 1981-02-23
Classification & Regulation
This clearance is catalogued under FDA product code KLE and 21 CFR 872.3200, within the Dental review panel as a Class II device.