Cleared Traditional

K092756 - GE VSCAN COMPACT DIAGNOSTIC ULTRASOUND ...

K092756 is an FDA 510(k) clearance for GE VSCAN COMPACT DIAGNOSTIC ULTRASOUND ..., manufactured by Ge Vingmed Ultrasound AS. The device is a Class 2 Radiology device with product code ITX cleared through the Traditional 510(k) pathway after a 19-day FDA review.

K092756 · Ge Vingmed Ultrasound AS · Radiology device
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Sep 2009
Decision
19d
Days
Class 2
Risk

K092756 is an FDA 510(k) clearance for the GE VSCAN COMPACT DIAGNOSTIC ULTRASOUND SYSTEM. Classified as Transducer, Ultrasonic, Diagnostic (product code ITX), Class II - Special Controls.

Submitted by Ge Vingmed Ultrasound AS (Horten, NO). The FDA issued a Cleared decision on September 28, 2009 after a review of 19 days - a notably fast clearance cycle.

This device falls under the Radiology FDA review panel, regulated under 21 CFR 892.1570 - 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: Fast-track predicate clearance. Standard predicate reliance. The short review cycle indicates strong predicate alignment - the FDA found sufficient equivalence without extended technical review.

View all Ge Vingmed Ultrasound AS devices

FDA 510(k) Submission Details - K092756

510(k) Number K092756 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received September 09, 2009
Decision Date September 28, 2009
Days to Decision 19 days
Submission Type Traditional
Review Panel Radiology (RA)
Summary Summary PDF
Third-party Review Yes - reviewed by an FDA-accredited third party
Regulatory Context
Review time vs. panel average
88d faster than avg
Panel avg: 107d · This submission: 19d
Pathway characteristics
Predicate-based equivalence. No clinical trials required. Third-party reviewed.

ITX Device Classification - Class 2, Special Controls

Product Code ITX Transducer, Ultrasonic, Diagnostic
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 892.1570
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 - ITX Transducer, Ultrasonic, Diagnostic

All 241
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