Cleared Traditional

IFIS-SA INTEGRATED FUCTIONAL IMAGING SYSTEM (K003899) - FDA 510(k) Clearance

Class II Radiology device cleared through predicate-based substantial equivalence - typically does not require clinical trials.

K003899 · Mri Devices Corp. · Radiology device
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Mar 2001
Decision
87d
Days
Class 2
Risk

K003899 is an FDA 510(k) clearance for the IFIS-SA INTEGRATED FUCTIONAL IMAGING SYSTEM. Classified as System, Nuclear Magnetic Resonance Imaging (product code LNH), Class II - Special Controls.

Submitted by Mri Devices Corp. (Waukesha, US). The FDA issued a Cleared decision on March 15, 2001 after a review of 87 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 Mri Devices Corp. devices

Submission Details

510(k) Number K003899 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received December 18, 2000
Decision Date March 15, 2001
Days to Decision 87 days
Submission Type Traditional
Review Panel Radiology (RA)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
20d faster than avg
Panel avg: 107d · This submission: 87d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

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 475
Devices cleared under the same product code (LNH) and FDA review panel - the closest regulatory comparables to K003899.
BREAST BIOPSY DEVICE/MAGNETOM SYSTEMS
K010773 · Siemens Medical Solutions USA, Inc. · May 2001
BLOOD OXYGENATION LEVEL DEPENDENT (BOLD) OPTION
K010691 · Philips Medical Systems (Cleveland), Inc. · May 2001
FIESTA IMAGING OPTION
K002997 · GE Medical Systems · Apr 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