Cleared Traditional

K930045 - MODEL #QSC-200-21 20 CM. QUADRATURE SHO...

K930045 is the FDA 510(k) clearance for MODEL #QSC-200-21 20 CM. QUADRATURE SHO... by Mri Devices Corp.. It is a Class 2 Radiology device (product code LNH) cleared through the Traditional 510(k) pathway after a 202-day FDA review.

K930045 · Mri Devices Corp. · Radiology device
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Jul 1993
Decision
202d
Days
Class 2
Risk

K930045 is an FDA 510(k) clearance for the MODEL #QSC-200-21 20 CM. QUADRATURE SHOULDER COIL. 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 July 26, 1993 after a review of 202 days - an extended review 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: Standard predicate-based submission. Standard predicate reliance. This clearance follows a standard predicate-based equivalence path within the Radiology review framework, consistent with the majority of Class II 510(k) submissions.

View all Mri Devices Corp. devices

Submission Details

510(k) Number K930045 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received January 05, 1993
Decision Date July 26, 1993
Days to Decision 202 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
95d slower than avg
Panel avg: 107d · This submission: 202d
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

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