Clearance Summary
LASER - 1000 received FDA 510(k) clearance under submission number K882436, sponsored by Panoramic Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 1988-08-04.
- Submission: K882436
- Applicant / Sponsor: Panoramic Corp.
- Clearance pathway: Traditional
- Review panel: Dental
- Device class: Class II
- Regulation citation: 21 CFR 872.1800
- Decision date: 1988-08-04
Classification & Regulation
This clearance is catalogued under FDA product code EHD and 21 CFR 872.1800, within the Dental review panel as a Class II device.