Cleared Traditional

K920742 - HYDRAJUST IV UROLOGICAL TABLE

K920742 is the FDA 510(k) clearance for HYDRAJUST IV UROLOGICAL TABLE by Mallinckrodt Group, Inc.. It is a Class 2 Radiology device (product code IXR) cleared through the Traditional 510(k) pathway after a 68-day FDA review.

K920742 · Mallinckrodt Group, Inc. · Radiology device
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Apr 1992
Decision
68d
Days
Class 2
Risk

K920742 is an FDA 510(k) clearance for the HYDRAJUST IV UROLOGICAL TABLE. Classified as Table, Radiographic, Tilting (product code IXR), Class II - Special Controls.

Submitted by Mallinckrodt Group, Inc. (Cincinnati, US). The FDA issued a Cleared decision on April 27, 1992 after a review of 68 days - a notably fast clearance cycle.

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: Fast-track predicate clearance. Standard predicate reliance. The short review cycle indicates strong predicate alignment - the FDA found sufficient equivalence without extended technical review.

View all Mallinckrodt Group, Inc. devices

Submission Details

510(k) Number K920742 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received February 19, 1992
Decision Date April 27, 1992
Days to Decision 68 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
39d faster than avg
Panel avg: 107d · This submission: 68d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

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 34
Devices cleared under the same product code (IXR) and FDA review panel - the closest regulatory comparables to K920742.
DUA-900A IMAGE-INTENSIFIED FLUOROSCOPIC X-RAY SYST
K922364 · Toshiba America Medical Systems, In.C · Sep 1992
UROLOGICAL X-RAY TABLE HS-10A
K920726 · Shimadzu Medical Systems · May 1992
X-RAY DIAGNOSTIC TABLE YSF-100
K920728 · Shimadzu Medical Systems · May 1992
X-RAY DIAGNOSTIC TABLE YSF-200-30-90
K920722 · Shimadzu Medical Systems · Apr 1992
TANGENT V
K915853 · Fischer Imaging Corp. · Jan 1992
X-RAY TABLE
K914165 · Siemens Medical Solutions USA, Inc. · Nov 1991