K-number	K222855
Device name	Digital Radiography CXDI-Pro, Digital Radiography D1
Applicant	Canon, Inc.
Product code	MQB
Device class	Class II
Decision date	Oct 17, 2022
Decision	Substantially Equivalent
Regulation	892.1680

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Source

View the full FDA submission: accessdata.fda.gov

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Digital Radiography CXDI-Pro, Digital Radiography D1

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