Clearance Summary
FLOSS CARD received FDA 510(k) clearance under submission number K862694, sponsored by Floss Card 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 1986-08-06.
- Submission: K862694
- Applicant / Sponsor: Floss Card Co.
- Clearance pathway: Traditional
- Review panel: Dental
- Device class: Class I
- Regulation citation: 21 CFR 872.6390
- Decision date: 1986-08-06
Classification & Regulation
This clearance is catalogued under FDA product code JES and 21 CFR 872.6390, within the Dental review panel as a Class I device.