Clearance Summary
PORTABLE X-RAY SYSTEM, MODELS DIOX-602, PROX received FDA 510(k) clearance under submission number K082167, sponsored by Digimed Corporation. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2008-09-26.
- Submission: K082167
- Applicant / Sponsor: Digimed Corporation
- Clearance pathway: Traditional
- Review panel: Dental
- Device class: Class II
- Regulation citation: 21 CFR 872.1800
- Decision date: 2008-09-26
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.