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FDA 510(k)

SCATTER CORRECTION FOR CXDI SERIES

K-Number: K153312 · 2016-06-28

ApplicantCanon, Inc.
Decision Date2016-06-28
Product CodeMQB
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

SCATTER CORRECTION FOR CXDI SERIES is a medical device manufactured by Canon, Inc.. It received FDA 510(k) clearance on 2016-06-28 under approval number K153312. 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 SCATTER CORRECTION FOR CXDI SERIES?

SCATTER CORRECTION FOR CXDI SERIES is a medical device that received FDA 510(k) clearance on 2016-06-28. It is manufactured by Canon, Inc.. The 510(k) number is K153312.

When was SCATTER CORRECTION FOR CXDI SERIES approved by the FDA?

SCATTER CORRECTION FOR CXDI SERIES received FDA 510(k) clearance on 2016-06-28, under approval number K153312.

What company makes SCATTER CORRECTION FOR CXDI SERIES?

SCATTER CORRECTION FOR CXDI SERIES is manufactured by Canon, Inc..

What is the FDA product code for SCATTER CORRECTION FOR CXDI SERIES?

The FDA product code for SCATTER CORRECTION FOR CXDI SERIES is MQB.

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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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