Clearance Summary
ADD'L INDICATION FOR OCTYLDENT 2-OCTYL CRANOACRY. received FDA 510(k) clearance under submission number K902078, sponsored by Crx Medical, 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 1990-08-03.
- Submission: K902078
- Applicant / Sponsor: Crx Medical, Inc.
- Clearance pathway: Traditional
- Review panel: Dental
- Device class: Class II
- Regulation citation: 21 CFR 872.3275
- Decision date: 1990-08-03
Classification & Regulation
This clearance is catalogued under FDA product code EMA and 21 CFR 872.3275, within the Dental review panel as a Class II device.