Clearance Summary
REAMER TYPE K ENDODONTIC received FDA 510(k) clearance under submission number K823686, sponsored by United Dental Mfg., 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 1982-12-28.
- Submission: K823686
- Applicant / Sponsor: United Dental Mfg., Inc.
- Clearance pathway: Traditional
- Review panel: Dental
- Device class: Class I
- Regulation citation: 21 CFR 872.4565
- Decision date: 1982-12-28
Classification & Regulation
This clearance is catalogued under FDA product code EKP and 21 CFR 872.4565, within the Dental review panel as a Class I device.