Cleared Traditional

K954356 - COMPAX 90/15E

K954356 is an FDA 510(k) clearance for COMPAX 90/15E, manufactured by General Electric Co.. The device is a Class 2 Radiology device with product code IXR cleared through the Traditional 510(k) pathway after a 19-day FDA review.

K954356 · General Electric Co. · Radiology device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Oct 1995
Decision
19d
Days
Class 2
Risk

K954356 is an FDA 510(k) clearance for the COMPAX 90/15E. Classified as Table, Radiographic, Tilting (product code IXR), Class II - Special Controls.

Submitted by General Electric Co. (Milwaukee, US). The FDA issued a Cleared decision on October 7, 1995 after a review of 19 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 General Electric Co. devices

FDA 510(k) Submission Details - K954356

510(k) Number K954356 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received September 18, 1995
Decision Date October 07, 1995
Days to Decision 19 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
88d faster than avg
Panel avg: 107d · This submission: 19d
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 K954356.
FLUOROVIEW SERIES FLUOROSCOPIC TABLES
K965096 · U.S. Imaging Tables, Inc. · Jan 1997
TILTING RADIOGRAPHIC TABLE (REMOTE)
K963851 · Acoma Medical Imaging, Inc. · Jan 1997
TANGENT VI TABLE
K961022 · Fischer Imaging Corp. · May 1996
KOORDINAT M
K951176 · Siemens Medical Solutions USA, Inc. · Apr 1995
MOBILIX MOBILE X-RAY TABLE
K945842 · GE Medical Systems · Jan 1995
HYDRADJUST IV UROLOGICAL TABLE
K943581 · Mallinckrodt Group, Inc. · Jan 1995