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FDA 510(k)

SCATTER CORRECTION FOR CXDI SERIES

K-Number: K153312 · 2016-06-28

ApplicantCanon, Inc.
Decision Date2016-06-28
Product CodeMQB
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

SCATTER CORRECTION FOR CXDI SERIES is the device name listed in this FDA 510(k) record. The listed applicant is Canon, Inc.. It received FDA 510(k) clearance on 2016-06-28 under 510(k) number K153312. 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 SCATTER CORRECTION FOR CXDI SERIES?

SCATTER CORRECTION FOR CXDI SERIES is a medical device that received FDA 510(k) clearance on 2016-06-28. The listed applicant is Canon, Inc.. The 510(k) number is K153312.

When did SCATTER CORRECTION FOR CXDI SERIES receive FDA 510(k) clearance?

SCATTER CORRECTION FOR CXDI SERIES received FDA 510(k) clearance on 2016-06-28, under 510(k) number K153312.

Who is the listed applicant for SCATTER CORRECTION FOR CXDI SERIES?

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 SCATTER CORRECTION FOR CXDI SERIES?

The FDA product code for SCATTER CORRECTION FOR CXDI SERIES 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.

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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