DIGITAL RADIOGRAPHY CXDI-Pro, D1— 510(k) K212553

Substantially Equivalent

Canon, Inc.

FDA 510(k) clearance K212553 for DIGITAL RADIOGRAPHY CXDI-Pro, D1, Substantially Equivalent on 2021-09-09. Applicant: Canon, Inc..

Clearance details

Applicant: Canon, Inc.
Product code: Code MQB
Advisory panel: Radiology
Date received: 2021-08-13
Decision date: 2021-09-09
Decision: Substantially Equivalent
Clearance type: Special
Location: Kawasaki, JP

Download summary PDF View on FDA.gov ↗

Data sourced from openFDA. This site is unofficial and independent of the FDA.