Clearance Summary
UnicLine Mobile received FDA 510(k) clearance under submission number K150490, sponsored by Heka Dental A/S. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2015-04-17.
- Submission: K150490
- Applicant / Sponsor: Heka Dental A/S
- Clearance pathway: Traditional
- Review panel: Dental
- Device class: Class I
- Regulation citation: 21 CFR 872.6640
- Decision date: 2015-04-17
Classification & Regulation
This clearance is catalogued under FDA product code EIA and 21 CFR 872.6640, within the Dental review panel as a Class I device.