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FDA 510(k)

CANON, DIGITAL RADIOGRAPHY, MODEL CXDI-50G

K-Number: K031447 · 2003-05-21

ApplicantCanon, Inc.
Decision Date2003-05-21
Product CodeMQB
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

CANON, DIGITAL RADIOGRAPHY, MODEL CXDI-50G is the device name listed in this FDA 510(k) record. The listed applicant is Canon, Inc.. It received FDA 510(k) clearance on 2003-05-21 under 510(k) number K031447. 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 CANON, DIGITAL RADIOGRAPHY, MODEL CXDI-50G?

CANON, DIGITAL RADIOGRAPHY, MODEL CXDI-50G is a medical device that received FDA 510(k) clearance on 2003-05-21. The listed applicant is Canon, Inc.. The 510(k) number is K031447.

When did CANON, DIGITAL RADIOGRAPHY, MODEL CXDI-50G receive FDA 510(k) clearance?

CANON, DIGITAL RADIOGRAPHY, MODEL CXDI-50G received FDA 510(k) clearance on 2003-05-21, under 510(k) number K031447.

Who is the listed applicant for CANON, DIGITAL RADIOGRAPHY, MODEL CXDI-50G?

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 CANON, DIGITAL RADIOGRAPHY, MODEL CXDI-50G?

The FDA product code for CANON, DIGITAL RADIOGRAPHY, MODEL CXDI-50G is MQB.

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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.

K252503Intelligent NRK241049CANON Fundus Camera CR-10 (CR-10)K232298DIGITAL RADIOGRAPHY CXDI-RF Wireless BlK230175Digital Radiography CXDI-CS01K222855Digital Radiography CXDI-Pro, Digital Radiography D1K222687Digital Radiography CXDI-Elite, Digital Radiography E1

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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.

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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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