Cleared Traditional

K250110 - Diagnostic Ultrasound System (MX6) (FDA 510(k) Clearance)

Also includes:

Diagnostic Ultrasound System (MX6S) Diagnostic Ultrasound System (MX6T) Diagnostic Ultrasound System (MX6 Exp) Diagnostic Ultrasound System (MX6 Pro) Diagnostic Ultrasound System (MX6 Super) Diagnostic Ultrasound System (MXG) Diagnostic Ultrasound System (Emerus MX6) Diagnostic Ultrasound System (Emerus MX6 Exp) Diagnostic Ultrasound System (Anesus MX6) Diagnostic Ultrasound System (Anesus MX6 Exp) Diagnostic Ultrasound System (Crius MX6)

Class II Radiology device cleared through predicate-based substantial equivalence - typically does not require clinical trials.

K250110 · Shenzhen Mindray Bio-Medical Electronics Co., Ltd. · Radiology device

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May 2025

Decision

120d

Days

Class 2

Risk

K250110 is an FDA 510(k) clearance for the Diagnostic Ultrasound System (MX6). Classified as System, Imaging, Pulsed Doppler, Ultrasonic within the IYN classification (a category covering pulsed Doppler and ultrasound imaging systems), Class II - Special Controls.

Submitted by Shenzhen Mindray Bio-Medical Electronics Co., Ltd. (Shenzhen, CN). The FDA issued a Cleared decision on May 16, 2025 after a review of 120 days - within the typical 510(k) review window.

This device falls under the Radiology FDA review panel, regulated under 21 CFR 892.1550 - the FDA radiology and imaging software oversight framework. The Traditional 510(k) pathway establishes clearance through substantial equivalence to a legally marketed predicate device, without requiring clinical trial data.

Device pattern: Standard predicate-based submission. Standard predicate reliance. This clearance follows a standard predicate-based equivalence path within the Radiology review framework, consistent with the majority of Class II 510(k) submissions.

View all Shenzhen Mindray Bio-Medical Electronics Co., Ltd. devices

Submission Details

510(k) Number	K250110 FDA.gov
FDA Decision	Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received	January 16, 2025
Decision Date	May 16, 2025
Days to Decision	120 days
Submission Type	Traditional
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

13d slower than avg

Panel avg: 107d · This submission: 120d

Pathway characteristics

Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code	IYN System, Imaging, Pulsed Doppler, Ultrasonic
Device Class	Class 2 - Special Controls
CFR Regulation	21 CFR 892.1550

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.