Clearance Summary
PERIO-MED DENTAL FLOSS received FDA 510(k) clearance under submission number K944034, sponsored by Whitehill Oral Technologies, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 1995-07-25.
- Submission: K944034
- Applicant / Sponsor: Whitehill Oral Technologies, Inc.
- Clearance pathway: Traditional
- Review panel: Dental
- Device class: Class I
- Regulation citation: 21 CFR 872.6390
- Decision date: 1995-07-25
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.