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FDA 510(k)

CXDI-40EC

K-Number: K062221 · 2006-08-17

ApplicantCanon, Inc.
Decision Date2006-08-17
Product CodeMQB
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

CXDI-40EC is the device name listed in this FDA 510(k) record. The listed applicant is Canon, Inc.. It received FDA 510(k) clearance on 2006-08-17 under 510(k) number K062221. 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 CXDI-40EC?

CXDI-40EC is a medical device that received FDA 510(k) clearance on 2006-08-17. The listed applicant is Canon, Inc.. The 510(k) number is K062221.

When did CXDI-40EC receive FDA 510(k) clearance?

CXDI-40EC received FDA 510(k) clearance on 2006-08-17, under 510(k) number K062221.

Who is the listed applicant for CXDI-40EC?

The FDA 510(k) record lists Canon, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CXDI-40EC?

The FDA product code for CXDI-40EC is MQB.

Other records listing Canon, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

View all 41 devices →

Related Devices (Code: MQB)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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