Cleared Traditional

K841996 - MAXICAMERA 400T W/BODY CONTOUR TOMOGRA (FDA 510(k) Clearance)

Class I Radiology device.

K841996 · General Electric Co. · Radiology device
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Jul 1984
Decision
61d
Days
Class 1
Risk

K841996 is an FDA 510(k) clearance for the MAXICAMERA 400T W/BODY CONTOUR TOMOGRA. Classified as Scanner, Whole Body, Nuclear (product code JAM), Class I - General Controls.

Submitted by General Electric Co. (Walker, US). The FDA issued a Cleared decision on July 16, 1984 after a review of 61 days - a notably fast clearance cycle.

This device falls under the Radiology FDA review panel, regulated under 21 CFR 892.1330 - 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 K841996 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received May 16, 1984
Decision Date July 16, 1984
Days to Decision 61 days
Submission Type Traditional
Review Panel Radiology (RA)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
46d faster than avg
Panel avg: 107d · This submission: 61d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code JAM Scanner, Whole Body, Nuclear
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 892.1330
What this classification means

Class I devices are subject to general controls only and most are exempt from 510(k) premarket notification. They represent the lowest regulatory burden in the FDA device framework.