Clearance Summary
SET PP received FDA 510(k) clearance under submission number K073043, sponsored by Sdi , Ltd.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2007-12-14.
- Submission: K073043
- Applicant / Sponsor: Sdi , Ltd.
- Clearance pathway: Traditional
- Review panel: Dental
- Device class: Class II
- Regulation citation: 21 CFR 872.3275
- Decision date: 2007-12-14
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.