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FDA 510(k)

Digital Radiography CXDI-CS01

K-Number: K222661 · 2022-09-27

ApplicantCanon, Inc.
Decision Date2022-09-27
Product CodeMQB
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

Digital Radiography CXDI-CS01 is a medical device manufactured by Canon, Inc.. It received FDA 510(k) clearance on 2022-09-27 under approval number K222661. The device is classified under product code MQB. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Digital Radiography CXDI-CS01?

Digital Radiography CXDI-CS01 is a medical device that received FDA 510(k) clearance on 2022-09-27. It is manufactured by Canon, Inc.. The 510(k) number is K222661.

When was Digital Radiography CXDI-CS01 approved by the FDA?

Digital Radiography CXDI-CS01 received FDA 510(k) clearance on 2022-09-27, under approval number K222661.

What company makes Digital Radiography CXDI-CS01?

Digital Radiography CXDI-CS01 is manufactured by Canon, Inc..

What is the FDA product code for Digital Radiography CXDI-CS01?

The FDA product code for Digital Radiography CXDI-CS01 is MQB.

Other Devices by Canon, Inc.

K153312SCATTER CORRECTION FOR CXDI SERIES K171270DIGITAL RADIOGRAPHY CXDI-410C WIRELESS K171194AS-10, CXDI-401RF K170332DIGITAL RADIOGRAPHY CXDI-710C WIRELESS, DIGITAL RADIOGRAPHY CXDI-810C WIRELESS K192632DIGITAL RADIOGRAPHY CXDI-702C Wireless, DIGITAL RADIOGRAPHY CXDI-402C Wireless K182942Canon OCT-A1

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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