Cleared Traditional

K920726 - UROLOGICAL X-RAY TABLE HS-10A

K920726 is an FDA 510(k) clearance for UROLOGICAL X-RAY TABLE HS-10A, manufactured by Shimadzu Medical Systems. The device is a Class 2 Radiology device with product code IXR cleared through the Traditional 510(k) pathway after a 101-day FDA review.

K920726 · Shimadzu Medical Systems · Radiology device
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May 1992
Decision
101d
Days
Class 2
Risk

K920726 is an FDA 510(k) clearance for the UROLOGICAL X-RAY TABLE HS-10A. Classified as Table, Radiographic, Tilting (product code IXR), Class II - Special Controls.

Submitted by Shimadzu Medical Systems (Gardena, US). The FDA issued a Cleared decision on May 29, 1992 after a review of 101 days - within the typical 510(k) review window.

This device falls under the Radiology FDA review panel, regulated under 21 CFR 892.1980 - 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 Medical Systems devices

FDA 510(k) Submission Details - K920726

510(k) Number K920726 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received February 18, 1992
Decision Date May 29, 1992
Days to Decision 101 days
Submission Type Traditional
Review Panel Radiology (RA)
Summary Statement
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
6d faster than avg
Panel avg: 107d · This submission: 101d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

IXR Device Classification - Class 2, Special Controls

Product Code IXR Table, Radiographic, Tilting
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 892.1980
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 - IXR Table, Radiographic, Tilting

All 47
Devices cleared under the same product code (IXR) and FDA review panel - the closest regulatory comparables to K920726.
UROLOGICAL C-ARM TABLE, MODEL #056-450
K922591 · Biodan Medical Systems, Ltd. · Nov 1992
SHIMADZU X-RAY DIAGNOSTIC TABLE YSF-200 30/90
K925175 · Shimadzu Medical Systems · Nov 1992
DUA-900A IMAGE-INTENSIFIED FLUOROSCOPIC X-RAY SYST
K922364 · Toshiba America Medical Systems, In.C · Sep 1992
X-RAY DIAGNOSTIC TABLE YSF-100
K920728 · Shimadzu Medical Systems · May 1992
HYDRAJUST IV UROLOGICAL TABLE
K920742 · Mallinckrodt Group, Inc. · Apr 1992
X-RAY DIAGNOSTIC TABLE YSF-200-30-90
K920722 · Shimadzu Medical Systems · Apr 1992