Cleared Traditional

K003573 - DIFFUSION TENSOR IMAGING OPTION

K003573 is an FDA 510(k) clearance for DIFFUSION TENSOR IMAGING OPTION, manufactured by Ge Medical Systems, Inc.. The device is a Class 2 Radiology device with product code LNH cleared through the Traditional 510(k) pathway after a 64-day FDA review.

K003573 · Ge Medical Systems, Inc. · Radiology device
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Jan 2001
Decision
64d
Days
Class 2
Risk

K003573 is an FDA 510(k) clearance for the DIFFUSION TENSOR IMAGING OPTION. Classified as System, Nuclear Magnetic Resonance Imaging (product code LNH), Class II - Special Controls.

Submitted by Ge Medical Systems, Inc. (Milwaukee, US). The FDA issued a Cleared decision on January 23, 2001 after a review of 64 days - a notably fast clearance cycle.

This device falls under the Radiology FDA review panel, regulated under 21 CFR 892.1000 - 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 Medical Systems, Inc. devices

FDA 510(k) Submission Details - K003573

510(k) Number K003573 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received November 20, 2000
Decision Date January 23, 2001
Days to Decision 64 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
43d faster than avg
Panel avg: 107d · This submission: 64d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

LNH Device Classification - Class 2, Special Controls

Product Code LNH System, Nuclear Magnetic Resonance Imaging
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 892.1000
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 - LNH System, Nuclear Magnetic Resonance Imaging

All 840
Devices cleared under the same product code (LNH) and FDA review panel - the closest regulatory comparables to K003573.
IFIS-SA INTEGRATED FUCTIONAL IMAGING SYSTEM
K003899 · Mri Devices Corp. · Mar 2001
FUNCTIONAL BRAIN MAPPING OPTION FOR MRI
K003947 · GE Medical Systems · Mar 2001
INFINION 1.5T MR IMAGING SYSTEM, MODEL MRI 100
K003853 · Philips Medical Systems (Cleveland), Inc. · Feb 2001
MAGNETOM RHAPSODY SYSTEM
K003628 · Siemens Medical Solutions USA, Inc. · Jan 2001
GYROSCAN INTERA 3.0T
K003516 · Philips Medical Systems North America, Inc. · Dec 2000
MAGNETIC CONCERTO
K003192 · Siemens Medical Solutions USA, Inc. · Dec 2000