Cleared Traditional

K931313 - KONICA QX-130APLUS AUTOMATIC X-RAY FILM PROCESSOR

K931313 is an FDA 510(k) clearance for KONICA QX-130APLUS AUTOMATIC X-RAY FILM..., manufactured by Konica Medical Corp.. The device is a Class 2 Radiology device with product code IXW cleared through the Traditional 510(k) pathway after a 176-day FDA review.

K931313 · Konica Medical Corp. · Radiology device
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Sep 1993
Decision
176d
Days
Class 2
Risk

K931313 is an FDA 510(k) clearance for the KONICA QX-130APLUS AUTOMATIC X-RAY FILM PROCESSOR. Classified as Processor, Radiographic-film, Automatic (product code IXW), Class II - Special Controls.

Submitted by Konica Medical Corp. (Washington, US). The FDA issued a Cleared decision on September 7, 1993 after a review of 176 days - an extended review cycle.

This device falls under the Radiology FDA review panel, regulated under 21 CFR 892.1900 - 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 Konica Medical Corp. devices

FDA 510(k) Submission Details - K931313

510(k) Number K931313 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received March 15, 1993
Decision Date September 07, 1993
Days to Decision 176 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
69d slower than avg
Panel avg: 107d · This submission: 176d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

IXW Device Classification - Class 2, Special Controls

Product Code IXW Processor, Radiographic-film, Automatic
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 892.1900
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 - IXW Processor, Radiographic-film, Automatic

All 51
Devices cleared under the same product code (IXW) and FDA review panel - the closest regulatory comparables to K931313.
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