Cleared Traditional

K933472 - SHIMADZU DIGITAL SUBSTRACTION SYST DAR-2400 SERIES (FDA 510(k) Clearance)

Class II Radiology device cleared through predicate-based substantial equivalence - typically does not require clinical trials.

K933472 · Shimadzu Corp. · Radiology device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Feb 1994
Decision
207d
Days
Class 2
Risk

K933472 is an FDA 510(k) clearance for the SHIMADZU DIGITAL SUBSTRACTION SYST DAR-2400 SERIES. Classified as System, X-ray, Fluoroscopic, Image-intensified (product code JAA), Class II - Special Controls.

Submitted by Shimadzu Corp. (Kyoto City 604 Japan, JP). The FDA issued a Cleared decision on February 7, 1994 after a review of 207 days - an extended review cycle.

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 Shimadzu Corp. devices

Submission Details

510(k) Number K933472 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received July 15, 1993
Decision Date February 07, 1994
Days to Decision 207 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
100d slower than avg
Panel avg: 107d · This submission: 207d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code JAA System, X-ray, Fluoroscopic, Image-intensified
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 892.1650
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 - JAA System, X-ray, Fluoroscopic, Image-intensified

All 298
Devices cleared under the same product code (JAA) and FDA review panel - the closest regulatory comparables to K933472.
Insight Enhanced™ DRF (EN-1002-01)
K251650 · Imaging Engineering, LLC · Sep 2025
Soteria E-View
K242488 · Omega Medical Imaging, LLC · Jan 2025
Adora DRFi (04550010)
K242948 · Nrt X-Ray A/S · Dec 2024
TRIDENT Mobile Fluoroscopy System
K233380 · Dornier Medtech America · Jun 2024
ProxiDiagnost N90 / Precision CRF (706110, 706400)
K233945 · Philips Medical Systems Dmc GmbH · Jan 2024
CombiDiagnost R90
K232910 · Philips Medical Systems Dmc GmbH · Oct 2023