Digital Radiography CXDI-Pro, Digital Radiography D1— 510(k) K222855

Substantially Equivalent

Canon, Inc.

FDA 510(k) clearance K222855 for Digital Radiography CXDI-Pro, Digital Radiography D1, Substantially Equivalent on 2022-10-17. Applicant: Canon, Inc..

Clearance details

Applicant: Canon, Inc.
Product code: Code MQB
Advisory panel: Radiology
Date received: 2022-09-21
Decision date: 2022-10-17
Decision: Substantially Equivalent
Clearance type: Special
Location: Kawasaki, JP

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