Clearance Summary
HURRISEAL DENTIN DESENSITIZER received FDA 510(k) clearance under submission number K973002, sponsored by Cheng & Assoc., 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 1998-03-23.
- Submission: K973002
- Applicant / Sponsor: Cheng & Assoc., Inc.
- Clearance pathway: Traditional
- Review panel: Dental
- Device class: Class II
- Regulation citation: 21 CFR 872.3200
- Decision date: 1998-03-23
Classification & Regulation
This clearance is catalogued under FDA product code KLE and 21 CFR 872.3200, within the Dental review panel as a Class II device.