Cleared Traditional

K260190 - ARTHUR

K260190 is an FDA 510(k) clearance for ARTHUR, manufactured by ROPCA ApS. The device is a Class 2 Radiology device with product code IYO cleared through the Traditional 510(k) pathway after a 147-day FDA review.

K260190 · ROPCA ApS · Radiology device
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Optimized for regulatory review, auditing and printing
Jun 2026
Decision
147d
Days
Class 2
Risk

K260190 is an FDA 510(k) clearance for the ARTHUR. Classified as System, Imaging, Pulsed Echo, Ultrasonic (product code IYO), Class II - Special Controls.

Submitted by ROPCA ApS (Odense M, DK). The FDA issued a Cleared decision on June 18, 2026 after a review of 147 days - within the typical 510(k) review window.

This device falls under the Radiology FDA review panel, regulated under 21 CFR 892.1560 - 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 ROPCA ApS devices

FDA 510(k) Submission Details - K260190

510(k) Number K260190 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received January 22, 2026
Decision Date June 18, 2026
Days to Decision 147 days
Submission Type Traditional
Review Panel Radiology (RA)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
40d slower than avg
Panel avg: 107d · This submission: 147d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

IYO Device Classification - Class 2, Special Controls

Product Code IYO System, Imaging, Pulsed Echo, Ultrasonic
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 892.1560
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 - IYO System, Imaging, Pulsed Echo, Ultrasonic

All 453
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