Clearance Summary
DENCLENZ received FDA 510(k) clearance under submission number K854995, sponsored by Creighton Products 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 1986-05-12.
- Submission: K854995
- Applicant / Sponsor: Creighton Products Corp.
- Clearance pathway: Traditional
- Review panel: Dental
- Device class: Class I
- Regulation citation: 21 CFR 872.3520
- Decision date: 1986-05-12
Classification & Regulation
This clearance is catalogued under FDA product code EFT and 21 CFR 872.3520, within the Dental review panel as a Class I device.