Clearance Summary
PRO-KUP received FDA 510(k) clearance under submission number K770556, sponsored by Dental Control Products. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 1977-03-24.
- Submission: K770556
- Applicant / Sponsor: Dental Control Products
- Clearance pathway: Traditional
- Review panel: Dental
- Device class: Class I
- Regulation citation: 21 CFR 872.6290
- Decision date: 1977-03-24
Classification & Regulation
This clearance is catalogued under FDA product code EHK and 21 CFR 872.6290, within the Dental review panel as a Class I device.