Clearance Summary
ROOT CANAL POST received FDA 510(k) clearance under submission number K924376, sponsored by The Thera Group. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 1993-11-22.
- Submission: K924376
- Applicant / Sponsor: The Thera Group
- Clearance pathway: Traditional
- Review panel: Dental
- Device class: Class I
- Regulation citation: 21 CFR 872.3740
- Decision date: 1993-11-22
Classification & Regulation
This clearance is catalogued under FDA product code EBL and 21 CFR 872.3740, within the Dental review panel as a Class I device.