Cleared Traditional

K801320 - SFX-90 TABLE/SPOTFILMER W/FLUORICON L200

K801320 is the FDA 510(k) clearance for SFX-90 TABLE/SPOTFILMER W/FLUORICON L200 by General Electric Co.. It is a Class 2 Radiology device (product code JAA) cleared through the Traditional 510(k) pathway after a 48-day FDA review.

K801320 · General Electric Co. · Radiology device
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Jul 1980
Decision
48d
Days
Class 2
Risk

K801320 is an FDA 510(k) clearance for the SFX-90 TABLE/SPOTFILMER W/FLUORICON L200. Classified as System, X-ray, Fluoroscopic, Image-intensified (product code JAA), Class II - Special Controls.

Submitted by General Electric Co. (Mchenry, US). The FDA issued a Cleared decision on July 21, 1980 after a review of 48 days - a notably fast clearance cycle.

This device falls under the Radiology FDA review panel, regulated under 21 CFR 892.1650 - 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 K801320 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received June 03, 1980
Decision Date July 21, 1980
Days to Decision 48 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
59d faster than avg
Panel avg: 107d · This submission: 48d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code JAA System, X-ray, Fluoroscopic, Image-intensified
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 892.1650
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 - JAA System, X-ray, Fluoroscopic, Image-intensified

All 135
Devices cleared under the same product code (JAA) and FDA review panel - the closest regulatory comparables to K801320.
DIGITAL FLUOROGRAPHIC X-RAY SYSTEM
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K802150 · Adac Laboratories · Oct 1980
DIGITAL SUBTRACTION RADIOGRAPHY SYSTEM
K801948 · Technicare Corp. · Sep 1980
ORBITOR
K800639 · Philips Medical Systems (Cleveland), Inc. · May 1980
L/U ARM - NEURO - VASCULAR #B5080B
K791830 · General Electric Co. · Oct 1979
EVALUSKOP
K781711 · Siemens Corp. · Oct 1978