Clearance Summary
CANNON DIGITAL RADIOGRAPHY MODEL CXDI-40G received FDA 510(k) clearance under submission number K023750, sponsored by Canon USA, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2002-11-22.
- Submission: K023750
- Applicant / Sponsor: Canon USA, Inc.
- Clearance pathway: Traditional
- Review panel: Radiology
- Device class: Class II
- Regulation citation: 21 CFR 892.1680
- Decision date: 2002-11-22
Classification & Regulation
This clearance is catalogued under FDA product code MQB and 21 CFR 892.1680, within the Radiology review panel as a Class II device.