Clearance Summary
EVERSTICK POST received FDA 510(k) clearance under submission number K030820, sponsored by Stick Tech , 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 2003-05-20.
- Submission: K030820
- Applicant / Sponsor: Stick Tech , Ltd.
- Clearance pathway: Traditional
- Review panel: Dental
- Device class: Class I
- Regulation citation: 21 CFR 872.3810
- Decision date: 2003-05-20
Classification & Regulation
This clearance is catalogued under FDA product code ELR and 21 CFR 872.3810, within the Dental review panel as a Class I device.