Clearance Summary
DR FLOSSER REFILL received FDA 510(k) clearance under submission number K871392, sponsored by Flossrite Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 1987-04-15.
- Submission: K871392
- Applicant / Sponsor: Flossrite Corp.
- Clearance pathway: Traditional
- Review panel: Dental
- Device class: Class I
- Regulation citation: 21 CFR 872.6390
- Decision date: 1987-04-15
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.