Digital Radiography Cxdi-40g Compact

No FDA recalls on record, checked 22 Oct 2026.

510(k) Number

K090623 ↗

FDA Product Code

MQB

Device Class

Class II

Regulation

21 CFR Part 892.1680

Advisory Committee

Radiology

FDA Decision

SESE Substantially Equivalent

• Canon X-Ray Image Distributor Cxi-3-3D

  Class II

  FDA 510(k) K871119 Active Cleared 31 Mar 1987

• Canon 60 Fundus Camera Cf-60U

  Class II

  FDA 510(k) K843021 Active Cleared 5 Oct 1984

• Canon X-Ray Image Distributor

  Class II

  FDA 510(k) K853984 Active Cleared 16 Oct 1985

• Optional Probe of Canon IOL Estimator Ku-1

  Class II

  FDA 510(k) K891225 Active Cleared 31 May 1989

• Pacs Software Solution 2003

  Class II

  FDA 510(k) K033624 Active Cleared 15 Dec 2003

• Canon X-Ray I.I. Rapid Sequence Camera Crs-105

  Class I

  FDA 510(k) K853861 Active Cleared 24 Oct 1985

See all devices from Canon USA, Inc. →