CXDI-40EC
K-Number: K062221 · 2006-08-17
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Device Summary
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.
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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