Cleared Traditional

K854410 - VERIFLEX

K854410 is an FDA 510(k) clearance for VERIFLEX, manufactured by Old Delft Corp. of America. The device is a Class 2 Radiology device with product code KPZ cleared through the Traditional 510(k) pathway after a 103-day FDA review.

K854410 · Old Delft Corp. of America · Radiology device
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Feb 1986
Decision
103d
Days
Class 2
Risk

K854410 is an FDA 510(k) clearance for the VERIFLEX. Classified as Generator, High Voltage, X-ray, Therapeutic (product code KPZ), Class II - Special Controls.

Submitted by Old Delft Corp. of America (Fairfax, US). The FDA issued a Cleared decision on February 12, 1986 after a review of 103 days - within the typical 510(k) review window.

This device falls under the Radiology FDA review panel, regulated under 21 CFR 892.5900 - 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 Old Delft Corp. of America devices

FDA 510(k) Submission Details - K854410

510(k) Number K854410 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received November 01, 1985
Decision Date February 12, 1986
Days to Decision 103 days
Submission Type Traditional
Review Panel Radiology (RA)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
4d faster than avg
Panel avg: 107d · This submission: 103d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

KPZ Device Classification - Class 2, Special Controls

Product Code KPZ Generator, High Voltage, X-ray, Therapeutic
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 892.5900
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.