Cleared Traditional

K925858 - OE 1.5 SI

K925858 is an FDA 510(k) clearance for OE 1.5 SI, manufactured by Otsuka Electronics. The device is a Class 2 Radiology device with product code LNH cleared through the Traditional 510(k) pathway after a 380-day FDA review.

K925858 · Otsuka Electronics · Radiology device
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Dec 1993
Decision
380d
Days
Class 2
Risk

K925858 is an FDA 510(k) clearance for the OE 1.5 SI. Classified as System, Nuclear Magnetic Resonance Imaging (product code LNH), Class II - Special Controls.

Submitted by Otsuka Electronics (Fort Collins, US). The FDA issued a Cleared decision on December 2, 1993 after a review of 380 days - an unusually long review period, suggesting complex equivalence evaluation.

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. Elevated predicate reliance profile. 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 Otsuka Electronics devices

FDA 510(k) Submission Details - K925858

510(k) Number K925858 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received November 17, 1992
Decision Date December 02, 1993
Days to Decision 380 days
Submission Type Traditional
Review Panel Radiology (RA)
Summary Statement
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
273d slower than avg
Panel avg: 107d · This submission: 380d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

LNH Device Classification - Class 2, Special Controls

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 1005
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