Cleared Traditional

K820688 - ARRANGE TM

K820688 is the FDA 510(k) clearance for ARRANGE TM by General Electric Co.. It is a Class 2 Radiology device (product code JAK) cleared through the Traditional 510(k) pathway after a 19-day FDA review.

K820688 · General Electric Co. · Radiology device
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Mar 1982
Decision
19d
Days
Class 2
Risk

K820688 is an FDA 510(k) clearance for the ARRANGE TM. Classified as System, X-ray, Tomography, Computed (product code JAK), Class II - Special Controls.

Submitted by General Electric Co. (Mchenry, US). The FDA issued a Cleared decision on March 31, 1982 after a review of 19 days - a notably fast clearance cycle.

This device falls under the Radiology FDA review panel, regulated under 21 CFR 892.1750 - 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

Submission Details

510(k) Number K820688 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received March 12, 1982
Decision Date March 31, 1982
Days to Decision 19 days
Submission Type Traditional
Review Panel Radiology (RA)
Summary -
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.

Device Classification

Product Code JAK System, X-ray, Tomography, Computed
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 892.1750
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 - JAK System, X-ray, Tomography, Computed

All 604
Devices cleared under the same product code (JAK) and FDA review panel - the closest regulatory comparables to K820688.
CT 9000
K843927 · General Electric Co. · Dec 1984
CT 9800
K841997 · General Electric Co. · Sep 1984
CENTAURI CT SCANNER
K840860 · Technicare Corp. · May 1984
IMAGE ANALYSIS CENTER
K813196 · Technicare Corp. · Dec 1981
CT/T 8800
K812509 · General Electric Co. · Oct 1981
DELTASCAN 2060 CT SCANNER
K812410 · Technicare Corp. · Oct 1981