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FDA 510(k)

DIGITAL RADIOGRAPHY CXDI-40G COMPACT

K-Number: K090623 · 2009-03-24

ApplicantCanon USA, Inc.
Decision Date2009-03-24
Product CodeMQB
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

DIGITAL RADIOGRAPHY CXDI-40G COMPACT is the device name listed in this FDA 510(k) record. The listed applicant is Canon USA, Inc.. It received FDA 510(k) clearance on 2009-03-24 under 510(k) number K090623. 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-40G COMPACT?

DIGITAL RADIOGRAPHY CXDI-40G COMPACT is a medical device that received FDA 510(k) clearance on 2009-03-24. The listed applicant is Canon USA, Inc.. The 510(k) number is K090623.

When did DIGITAL RADIOGRAPHY CXDI-40G COMPACT receive FDA 510(k) clearance?

DIGITAL RADIOGRAPHY CXDI-40G COMPACT received FDA 510(k) clearance on 2009-03-24, under 510(k) number K090623.

Who is the listed applicant for DIGITAL RADIOGRAPHY CXDI-40G COMPACT?

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

What is the FDA product code for DIGITAL RADIOGRAPHY CXDI-40G COMPACT?

The FDA product code for DIGITAL RADIOGRAPHY CXDI-40G COMPACT is MQB.

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Other records listing Canon USA, 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.

K033624PACS SOFTWARE SOLUTION 2003K031633CANON INC., DIGITAL RADIOGRAPHY, MODEL CXDI-40CK031629CANON NON-MYDRIATIC RETINAL CAMERA, MODEL CR-DGIK023750CANNON DIGITAL RADIOGRAPHY MODEL CXDI-40GK023586DR-ER VERFSION OF CANON X-RAY DIGITAL CAMERASK003689CANON X-RAY DIGITAL CAMERA, MODEL CXDI-31

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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.

K2538000909FCE, 0909FCE-HSRayence Co., Ltd.K260820VIVIX-S 4386W (FXRD-4386WA)Vieworks Co., Ltd.K252996Universal 1417PIKonica Minolta Healthcare Americas, Inc.K252911Lux HD 2530 detector (Lux HD 2530)Iray Imaging Technology (Haining) LimitedK250211Yushan X-Ray Flat Panel DetectorInnocare Optoelectronics Corp.K250665SKR 3000Konica Minolta, Inc.

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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