Cleared Abbreviated

K172931 - DUS-6000 Digital Ultrasonic Diagnostic ...

K172931 is the FDA 510(k) clearance for DUS-6000 Digital Ultrasonic Diagnostic ... by Advanced Instrumentations, Inc.. It is a Class 2 Radiology device (product code IYO) cleared through the Abbreviated 510(k) pathway after a 67-day FDA review.

K172931 · Advanced Instrumentations, Inc. · Radiology device
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Dec 2017
Decision
67d
Days
Class 2
Risk

K172931 is an FDA 510(k) clearance for the DUS-6000 Digital Ultrasonic Diagnostic Imaging System. Classified as System, Imaging, Pulsed Echo, Ultrasonic (product code IYO), Class II - Special Controls.

Submitted by Advanced Instrumentations, Inc. (Miami, US). The FDA issued a Cleared decision on December 1, 2017 after a review of 67 days - a notably fast clearance cycle.

This device falls under the Radiology FDA review panel, regulated under 21 CFR 892.1560 - the FDA radiology and imaging software oversight framework. The Abbreviated 510(k) pathway was used, relying on FDA-recognized standards to demonstrate substantial equivalence.

Device pattern: Standards-based predicate clearance. Standards-verified equivalence. The Abbreviated pathway signals strong alignment with FDA-recognized performance standards - typically associated with lower review burden and faster clearance cycles.

View all Advanced Instrumentations, Inc. devices

Submission Details

510(k) Number K172931 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received September 25, 2017
Decision Date December 01, 2017
Days to Decision 67 days
Submission Type Abbreviated
Review Panel Radiology (RA)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
40d faster than avg
Panel avg: 107d · This submission: 67d
Pathway characteristics
Standards-based clearance path.

Device Classification

Product Code IYO System, Imaging, Pulsed Echo, Ultrasonic
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 892.1560
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 - IYO System, Imaging, Pulsed Echo, Ultrasonic

All 395
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