Cleared Traditional

K801986 - DATASON DB SYSTEM

K801986 is the FDA 510(k) clearance for DATASON DB SYSTEM by General Electric Co.. It is a Class 2 Radiology device (product code IYO) cleared through the Traditional 510(k) pathway after a 85-day FDA review.

K801986 · General Electric Co. · Radiology device
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Nov 1980
Decision
85d
Days
Class 2
Risk

K801986 is an FDA 510(k) clearance for the DATASON DB SYSTEM. Classified as System, Imaging, Pulsed Echo, Ultrasonic (product code IYO), Class II - Special Controls.

Submitted by General Electric Co. (Mchenry, US). The FDA issued a Cleared decision on November 12, 1980 after a review of 85 days - a notably fast clearance cycle.

This device falls under the Radiology FDA review panel, regulated under 21 CFR 892.1560 - 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 K801986 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received August 19, 1980
Decision Date November 12, 1980
Days to Decision 85 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
22d faster than avg
Panel avg: 107d · This submission: 85d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code IYO System, Imaging, Pulsed Echo, Ultrasonic
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 892.1560
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 - IYO System, Imaging, Pulsed Echo, Ultrasonic

All 408
Devices cleared under the same product code (IYO) and FDA review panel - the closest regulatory comparables to K801986.
SYSTEM, ECHO, PULSED ULTRASONIC DIAG.
K802708 · General Electric Co. · Jan 1981
SIEMENS PHO/SONIC ALPHA 1000
K802759 · Siemens Gammasonics, Inc. · Jan 1981
HP MODEL 77020A ULTRASOUND SYSTEM
K801954 · Hewlett-Packard Co. · Dec 1980
MINIVISOR TERMINAL
K802263 · Organon Teknika Corp. · Oct 1980
DATASON RTL
K801454 · General Electric Co. · Sep 1980
MARK V DUPLEX ULTRASONIC SCANNING SYSTEM
K801598 · Advanced Technology Laboratories, Inc. · Aug 1980