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FDA 510(k)

DIGITAL RADIOGRAPHY CXDI-410C WIRELESS

K-Number: K171270 · 2017-11-17

ApplicantCanon, Inc.
Decision Date2017-11-17
Product CodeMQB
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

DIGITAL RADIOGRAPHY CXDI-410C WIRELESS is a medical device manufactured by Canon, Inc.. It received FDA 510(k) clearance on 2017-11-17 under approval number K171270. 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-410C WIRELESS?

DIGITAL RADIOGRAPHY CXDI-410C WIRELESS is a medical device that received FDA 510(k) clearance on 2017-11-17. It is manufactured by Canon, Inc.. The 510(k) number is K171270.

When was DIGITAL RADIOGRAPHY CXDI-410C WIRELESS approved by the FDA?

DIGITAL RADIOGRAPHY CXDI-410C WIRELESS received FDA 510(k) clearance on 2017-11-17, under approval number K171270.

What company makes DIGITAL RADIOGRAPHY CXDI-410C WIRELESS?

DIGITAL RADIOGRAPHY CXDI-410C WIRELESS is manufactured by Canon, Inc..

What is the FDA product code for DIGITAL RADIOGRAPHY CXDI-410C WIRELESS?

The FDA product code for DIGITAL RADIOGRAPHY CXDI-410C WIRELESS is MQB.

Other Devices by Canon, Inc.

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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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