Cleared Special

K013723 - MODIFICATION TO: EUB-6500 DIAGNOSTIC UL...

K013723 is the FDA 510(k) clearance for MODIFICATION TO: EUB-6500 DIAGNOSTIC UL... by Hitachi Medical Corp.. It is a Class 2 Radiology device (product code ITX) cleared through the Special 510(k) pathway after a 89-day FDA review.

K013723 · Hitachi Medical Corp. · Radiology device
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Feb 2002
Decision
89d
Days
Class 2
Risk

K013723 is an FDA 510(k) clearance for the MODIFICATION TO: EUB-6500 DIAGNOSTIC ULTRASOUND SCANNER. Classified as Transducer, Ultrasonic, Diagnostic (product code ITX), Class II - Special Controls.

Submitted by Hitachi Medical Corp. (Tarrytown, US). The FDA issued a Cleared decision on February 6, 2002 after a review of 89 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. As a Special 510(k), this submission covers a manufacturer modification to an existing cleared device rather than a new device introduction.

Device pattern: Iterative device modification. Low regulatory complexity profile. This Special 510(k) clearance confirms that the manufacturer's modifications remained within the established regulatory envelope of the original cleared device.

View all Hitachi Medical Corp. devices

Submission Details

510(k) Number K013723 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received November 09, 2001
Decision Date February 06, 2002
Days to Decision 89 days
Submission Type Special
Review Panel Radiology (RA)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
18d faster than avg
Panel avg: 107d · This submission: 89d
Pathway characteristics
Modification to existing cleared device.

Device Classification

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 203
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