Cleared Traditional

K942175 - LINEAR TOMOGRAPHIC SYSTEM: PMT 6000

K942175 is an FDA 510(k) clearance for LINEAR TOMOGRAPHIC SYSTEM: PMT 6000, manufactured by Continental X-Ray Corp.. The device is a Class 2 Radiology device with product code IZF cleared through the Traditional 510(k) pathway after a 105-day FDA review.

K942175 · Continental X-Ray Corp. · Radiology device
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Aug 1994
Decision
105d
Days
Class 2
Risk

K942175 is an FDA 510(k) clearance for the LINEAR TOMOGRAPHIC SYSTEM: PMT 6000. Classified as System, X-ray, Tomographic (product code IZF), Class II - Special Controls.

Submitted by Continental X-Ray Corp. (Broadview, US). The FDA issued a Cleared decision on August 17, 1994 after a review of 105 days - within the typical 510(k) review window.

This device falls under the Radiology FDA review panel, regulated under 21 CFR 892.1740 - 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 Continental X-Ray Corp. devices

FDA 510(k) Submission Details - K942175

510(k) Number K942175 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received May 04, 1994
Decision Date August 17, 1994
Days to Decision 105 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
2d faster than avg
Panel avg: 107d · This submission: 105d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

IZF Device Classification - Class 2, Special Controls

Product Code IZF System, X-ray, Tomographic
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 892.1740
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 - IZF System, X-ray, Tomographic

All 26
Devices cleared under the same product code (IZF) and FDA review panel - the closest regulatory comparables to K942175.
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