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FDA 510(k)

EZSensor XHD

K-Number: K232255 · 2023-09-27

ApplicantQpix Solutions, Inc.
Decision Date2023-09-27
Product CodeMUH
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

EZSensor XHD is a medical device manufactured by Qpix Solutions, Inc.. It received FDA 510(k) clearance on 2023-09-27 under approval number K232255. The device is classified under product code MUH. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EZSensor XHD?

EZSensor XHD is a medical device that received FDA 510(k) clearance on 2023-09-27. It is manufactured by Qpix Solutions, Inc.. The 510(k) number is K232255.

When was EZSensor XHD approved by the FDA?

EZSensor XHD received FDA 510(k) clearance on 2023-09-27, under approval number K232255.

What company makes EZSensor XHD?

EZSensor XHD is manufactured by Qpix Solutions, Inc..

What is the FDA product code for EZSensor XHD?

The FDA product code for EZSensor XHD is MUH.

Other Devices by Qpix Solutions, Inc.

K242778X Sensor (Model: IOS-A15IF, HDI-15DGF) K252570EzSensor HD, EzSensor UHD

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K162619I View and Imagen SensorTrident S.R.L K162585SuniIQ Digital Radiography SystemSuni Medical Imaging, Inc. K161131FONA Pan/CephFona S.R.L K160788RIOScan (RPS500)Ray Co., Ltd. K160386ReadeR, VieweR, QuickScan PSPTrident S.R.L K153144TIO-H DIGITAL RADIOGRAPHY SENSORDenttio, 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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