Cleared Special

K230175 - Digital Radiography CXDI-CS01

K230175 is the FDA 510(k) clearance for Digital Radiography CXDI-CS01 by Canon, Inc.. It is a Class 2 Radiology device (product code MQB) cleared through the Special 510(k) pathway after a 26-day FDA review.

K230175 · Canon, Inc. · Radiology device
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Feb 2023
Decision
26d
Days
Class 2
Risk

K230175 is an FDA 510(k) clearance for the Digital Radiography CXDI-CS01. Classified as Solid State X-ray Imager (flat Panel/digital Imager) (product code MQB), Class II - Special Controls.

Submitted by Canon, Inc. (Kawasaki, JP). The FDA issued a Cleared decision on February 15, 2023 after a review of 26 days - a notably fast clearance cycle.

This device falls under the Radiology FDA review panel, regulated under 21 CFR 892.1680 - the FDA radiology and imaging software oversight framework. As a Special 510(k), this submission covers a manufacturer modification to an existing cleared device rather than a new device introduction.

Device pattern: Iterative device modification. Low regulatory complexity profile. This Special 510(k) clearance confirms that the manufacturer's modifications remained within the established regulatory envelope of the original cleared device.

View all Canon, Inc. devices

Submission Details

510(k) Number K230175 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received January 20, 2023
Decision Date February 15, 2023
Days to Decision 26 days
Submission Type Special
Review Panel Radiology (RA)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
81d faster than avg
Panel avg: 107d · This submission: 26d
Pathway characteristics
Modification to existing cleared device.

Device Classification

Product Code MQB Solid State X-ray Imager (flat Panel/digital Imager)
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 892.1680
What this classification means

Class II devices require demonstration of substantial equivalence to a legally marketed predicate device. This pathway does not require clinical trials - it relies on engineering equivalence and performance data. Most Radiology devices follow this clearance model.

Regulatory Peers - MQB Solid State X-ray Imager (flat Panel/digital Imager)

All 218
Devices cleared under the same product code (MQB) and FDA review panel - the closest regulatory comparables to K230175.
AcuityDR 1013 G4, AcuityDR 1417 G4, AcuityDR 1717G4
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14HQ721G-B
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