Clearance Summary
LeEject 2 Dental Syringe and Needle System received FDA 510(k) clearance under submission number K171254, sponsored by Advanced Technology and Capital, 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 2017-11-16.
- Submission: K171254
- Applicant / Sponsor: Advanced Technology and Capital, Inc.
- Clearance pathway: Traditional
- Review panel: Dental
- Device class: Class II
- Regulation citation: 21 CFR 872.6770
- Decision date: 2017-11-16
Classification & Regulation
This clearance is catalogued under FDA product code EJI and 21 CFR 872.6770, within the Dental review panel as a Class II device.