Cleared Traditional

K020850 - GPF-29 GENERAL PURPOSE COIL SET

K020850 is the FDA 510(k) clearance for GPF-29 GENERAL PURPOSE COIL SET by Mri Devices Corp.. It is a Class 2 Radiology device (product code MOS) cleared through the Traditional 510(k) pathway after a 83-day FDA review.

K020850 · Mri Devices Corp. · Radiology device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Jun 2002
Decision
83d
Days
Class 2
Risk

K020850 is an FDA 510(k) clearance for the GPF-29 GENERAL PURPOSE COIL SET. Classified as Coil, Magnetic Resonance, Specialty (product code MOS), Class II - Special Controls.

Submitted by Mri Devices Corp. (Waukesha, US). The FDA issued a Cleared decision on June 6, 2002 after a review of 83 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 K020850 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received March 15, 2002
Decision Date June 06, 2002
Days to Decision 83 days
Submission Type Traditional
Review Panel Radiology (RA)
Summary Statement
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
24d faster than avg
Panel avg: 107d · This submission: 83d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

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 311
Devices cleared under the same product code (MOS) and FDA review panel - the closest regulatory comparables to K020850.
MODEL 415PH-64/42: PHASED ARRAY SHOULDER COIL
K021433 · Medical Advances, Inc. · Jun 2002
HNC-127-TRIO NEUROVASCULAR ARRAY COIL
K021570 · Mri Devices Corp. · Jun 2002
OBC-127 BREAST ARRAY COIL
K021575 · Mri Devices Corp. · Jun 2002
MAGNETOM SYMPHONY QUADRATURE TX/RX HEAD COIL
K021262 · Usa Instruments, Inc. · May 2002
NVA-63-8 NEUROVASCULAR ARRAY COIL
K020606 · Mri Devices Corp. · Mar 2002
MARK 5000 QUADRATURE SHOULDER COIL
K013854 · Usa Instruments, Inc. · Feb 2002