Cleared Traditional

K901384 - MODEL 6000-21

Also marketed or referenced as:
VOLUME NECK COIL

K901384 is an FDA 510(k) clearance for MODEL 6000-21, manufactured by Medical Advances, Inc.. The device is a Class 2 Radiology device with product code LNH cleared through the Traditional 510(k) pathway after a 31-day FDA review.

K901384 · Medical Advances, Inc. · Radiology device
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Apr 1990
Decision
31d
Days
Class 2
Risk

K901384 is an FDA 510(k) clearance for the MODEL 6000-21. Classified as System, Nuclear Magnetic Resonance Imaging (product code LNH), Class II - Special Controls.

Submitted by Medical Advances, Inc. (Milwaukee, US). The FDA issued a Cleared decision on April 26, 1990 after a review of 31 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 Medical Advances, Inc. devices

Submission Details

510(k) Number K901384 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received March 26, 1990
Decision Date April 26, 1990
Days to Decision 31 days
Submission Type Traditional
Review Panel Radiology (RA)
Summary -
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
76d faster than avg
Panel avg: 107d · This submission: 31d
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 817
Devices cleared under the same product code (LNH) and FDA review panel - the closest regulatory comparables to K901384.
MODEL 4050-64
K901639 · Medical Advances, Inc. · May 1990
MODEL 2121-64
K901242 · Medical Advances, Inc. · Apr 1990
MODEL 2121-21, TMJ SURFACE COIL
K901305 · Medical Advances, Inc. · Apr 1990
THORACIC/LUMBAR SPINE 8 RACETRACK COIL, 3080-64
K901241 · Medical Advances, Inc. · Apr 1990
MODEL 8010
K901092 · Medical Advances, Inc. · Apr 1990
MAGNETIC RESONANCE DIAGNOSTIC DEVICE ACCESSORIES
K900889 · Siemens Medical Solutions USA, Inc. · Mar 1990