Clearance Summary
KEN'S PROPHY GEL - REGULAR received FDA 510(k) clearance under submission number K896661, sponsored by Pulpdent 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 1990-02-14.
- Submission: K896661
- Applicant / Sponsor: Pulpdent Corp.
- Clearance pathway: Traditional
- Review panel: Dental
- Device class: Class I
- Regulation citation: 21 CFR 872.6030
- Decision date: 1990-02-14
Classification & Regulation
This clearance is catalogued under FDA product code EJR and 21 CFR 872.6030, within the Dental review panel as a Class I device.