Cleared Abbreviated

K031119 - MAYO CLINIC BC-10 1.5T

K031119 is an FDA 510(k) clearance for MAYO CLINIC BC-10 1.5T, manufactured by Mayo Medical Ventures. The device is a Class 2 Radiology device with product code MOS cleared through the Abbreviated 510(k) pathway after a 98-day FDA review.

K031119 · Mayo Medical Ventures · Radiology device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Jul 2003
Decision
98d
Days
Class 2
Risk

K031119 is an FDA 510(k) clearance for the MAYO CLINIC BC-10 1.5T. Classified as Coil, Magnetic Resonance, Specialty (product code MOS), Class II - Special Controls.

Submitted by Mayo Medical Ventures (Rochester, US). The FDA issued a Cleared decision on July 15, 2003 after a review of 98 days - within the typical 510(k) review window.

This device falls under the Radiology FDA review panel, regulated under 21 CFR 892.1000 - the FDA radiology and imaging software oversight framework. The Abbreviated 510(k) pathway was used, relying on FDA-recognized standards to demonstrate substantial equivalence.

Device pattern: Standards-based predicate clearance. Standards-verified equivalence. The Abbreviated pathway signals strong alignment with FDA-recognized performance standards - typically associated with lower review burden and faster clearance cycles.

View all Mayo Medical Ventures devices

FDA 510(k) Submission Details - K031119

510(k) Number K031119 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received April 08, 2003
Decision Date July 15, 2003
Days to Decision 98 days
Submission Type Abbreviated
Review Panel Radiology (RA)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
9d faster than avg
Panel avg: 107d · This submission: 98d
Pathway characteristics
Standards-based clearance path.

MOS Device Classification - Class 2, Special Controls

Product Code MOS Coil, Magnetic Resonance, Specialty
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 - MOS Coil, Magnetic Resonance, Specialty

All 385
Devices cleared under the same product code (MOS) and FDA review panel - the closest regulatory comparables to K031119.
QSC-127 SHOULDER ARRAY COIL SET
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PRIMA III TOTALSENSE TORSO COIL
K031365 · Usa Instruments, Inc. · Jul 2003
PREMIER 9000 8 CHANNEL PHASED ARRAY CTL SPINE COIL
K031366 · Usa Instruments, Inc. · Jul 2003
SENSE BODY COIL
K031095 · Philips Medical Systems (Cleveland), Inc. · Jun 2003
PREMIER III PHASED ARRAY CTL SPINE COIL
K031139 · Usa Instruments, Inc. · May 2003