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FDA 510(k)

DIGITAL RADIOGRAPHY MODEL CXDI-55G

K-Number: K091435 · 2009-05-29

ApplicantCanon, Inc.
Decision Date2009-05-29
Product CodeMQB
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

DIGITAL RADIOGRAPHY MODEL CXDI-55G is the device name listed in this FDA 510(k) record. The listed applicant is Canon, Inc.. It received FDA 510(k) clearance on 2009-05-29 under 510(k) number K091435. 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 MODEL CXDI-55G?

DIGITAL RADIOGRAPHY MODEL CXDI-55G is a medical device that received FDA 510(k) clearance on 2009-05-29. The listed applicant is Canon, Inc.. The 510(k) number is K091435.

When did DIGITAL RADIOGRAPHY MODEL CXDI-55G receive FDA 510(k) clearance?

DIGITAL RADIOGRAPHY MODEL CXDI-55G received FDA 510(k) clearance on 2009-05-29, under 510(k) number K091435.

Who is the listed applicant for DIGITAL RADIOGRAPHY MODEL CXDI-55G?

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 DIGITAL RADIOGRAPHY MODEL CXDI-55G?

The FDA product code for DIGITAL RADIOGRAPHY MODEL CXDI-55G 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.

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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