Cleared Special

K042739 - HI-ART SYSTEM

K042739 is an FDA 510(k) clearance for HI-ART SYSTEM, manufactured by Tomotherapy Incorporated. The device is a Class 2 Radiology device with product code MUJ cleared through the Special 510(k) pathway after a 30-day FDA review.

K042739 · Tomotherapy Incorporated · Radiology device
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Optimized for regulatory review, auditing and printing
Nov 2004
Decision
30d
Days
Class 2
Risk

K042739 is an FDA 510(k) clearance for the HI-ART SYSTEM. Classified as System, Planning, Radiation Therapy Treatment (product code MUJ), Class II - Special Controls.

Submitted by Tomotherapy Incorporated (Madison, US). The FDA issued a Cleared decision on November 3, 2004 after a review of 30 days - a notably fast clearance cycle.

This device falls under the Radiology FDA review panel, regulated under 21 CFR 892.5050 - 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 Tomotherapy Incorporated devices

FDA 510(k) Submission Details - K042739

510(k) Number K042739 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received October 04, 2004
Decision Date November 03, 2004
Days to Decision 30 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
77d faster than avg
Panel avg: 107d · This submission: 30d
Pathway characteristics
Modification to existing cleared device.

MUJ Device Classification - Class 2, Special Controls

Product Code MUJ System, Planning, Radiation Therapy Treatment
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 892.5050
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 - MUJ System, Planning, Radiation Therapy Treatment

All 161
Devices cleared under the same product code (MUJ) and FDA review panel - the closest regulatory comparables to K042739.
ECLIPSE TREATMENT PLANNING SYSTEM
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ECLIPSE WITH AAA
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ONCENTRA-VISIR
K041719 · Nucletron Corp. · Jul 2004