Cleared Traditional

K253752 - ARTIS genio floor

Also marketed or referenced as:
ARTIS icono.explore floor

K253752 is an FDA 510(k) clearance for ARTIS genio floor, manufactured by Siemens Medical Solutions USA, Inc.. The device is a Class 2 Radiology device with product code OWB cleared through the Traditional 510(k) pathway after a 149-day FDA review.

K253752 · Siemens Medical Solutions USA, Inc. · Radiology device
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Apr 2026
Decision
149d
Days
Class 2
Risk

K253752 is an FDA 510(k) clearance for the ARTIS genio floor. Classified as Interventional Fluoroscopic X-ray System (product code OWB), Class II - Special Controls.

Submitted by Siemens Medical Solutions USA, Inc. (Malvern, US). The FDA issued a Cleared decision on April 23, 2026 after a review of 149 days - within the typical 510(k) review window.

This device falls under the Radiology FDA review panel, regulated under 21 CFR 892.1650 - 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 Siemens Medical Solutions USA, Inc. devices

FDA 510(k) Submission Details - K253752

510(k) Number K253752 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received November 25, 2025
Decision Date April 23, 2026
Days to Decision 149 days
Submission Type Traditional
Review Panel Radiology (RA)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
42d slower than avg
Panel avg: 107d · This submission: 149d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

OWB Device Classification - Class 2, Special Controls

Product Code OWB Interventional Fluoroscopic X-ray System
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 892.1650
Definition Interventional Fluoroscopy
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 - OWB Interventional Fluoroscopic X-ray System

All 292
Devices cleared under the same product code (OWB) and FDA review panel - the closest regulatory comparables to K253752.
C-beam
K252735 · Pulmera, Inc. · May 2026
Intelligent NR
K252503 · Canon, Inc. · Apr 2026
ARTIS icono floor
K254173 · Siemens Medical Solutions USA, Inc. · Apr 2026
BELLIGER ACE
K252229 · Genoray Co., Ltd. · Apr 2026
Trinias
K252099 · Shimadzu Corporation · Mar 2026
Alphenix, INFX-8000V/B, INFX-8000V/S, V9.6 with aEvolve Imaging (FOV Extension)
K253584 · Canon Medical Systems Corporation · Mar 2026