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FDA 510(k)

EZSensor XHD

K-Number: K232255 · 2023-09-27

Decision Date2023-09-27
Product CodeMUH
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

EZSensor XHD is the device name listed in this FDA 510(k) record. The listed applicant is Qpix Solutions, Inc.. It received FDA 510(k) clearance on 2023-09-27 under 510(k) 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. The listed applicant is Qpix Solutions, Inc.. The 510(k) number is K232255.

When did EZSensor XHD receive FDA 510(k) clearance?

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

Who is the listed applicant for EZSensor XHD?

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

What is the FDA product code for EZSensor XHD?

The FDA product code for EZSensor XHD is MUH.

Other records listing Qpix Solutions, 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.

Related Devices (Code: MUH)

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.

Official Source

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