Cleared Special

GE LOGIQ 9, MODELS 2188900, 2375600, 2404587 AND 5150000 (K061129) - FDA 510(k) Clearance

Class II Radiology device cleared through the Special 510(k) pathway - typically does not require clinical trials.

K061129 · General Electric Co. · Radiology device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Jun 2006
Decision
38d
Days
Class 2
Risk

K061129 is an FDA 510(k) clearance for the GE LOGIQ 9, MODELS 2188900, 2375600, 2404587 AND 5150000. Classified as System, Imaging, Pulsed Doppler, Ultrasonic within the IYN classification (a category covering pulsed Doppler and ultrasound imaging systems), Class II - Special Controls.

Submitted by General Electric Co. (Wauwatosa, US). The FDA issued a Cleared decision on June 1, 2006 after a review of 38 days - a notably fast clearance cycle.

This device falls under the Radiology FDA review panel, regulated under 21 CFR 892.1550 - the FDA radiology and imaging software oversight framework. As a Special 510(k), this submission covers a manufacturer modification to an existing cleared device rather than a new device introduction.

Device pattern: Iterative device modification. Low regulatory complexity profile. This Special 510(k) clearance confirms that the manufacturer's modifications remained within the established regulatory envelope of the original cleared device.

View all General Electric Co. devices

Submission Details

510(k) Number K061129 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received April 24, 2006
Decision Date June 01, 2006
Days to Decision 38 days
Submission Type Special
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
69d faster than avg
Panel avg: 107d · This submission: 38d
Pathway characteristics
Modification to existing cleared device.

Device Classification

Product Code IYN System, Imaging, Pulsed Doppler, Ultrasonic
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 892.1550
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 - IYN System, Imaging, Pulsed Doppler, Ultrasonic

All 534
Devices cleared under the same product code (IYN) and FDA review panel - the closest regulatory comparables to K061129.
SIEMENS ACUSON X500 ULTRASOUND SYSTEM
K061980 · Siemens Medical Solutions USA, Inc. · Aug 2006
ACUSON X300 DIAGNOSTIC ULTRASOUND SYSTEM
K061946 · Siemens Medical Solutions USA, Inc. · Jul 2006
GE VIVID - I
K061525 · General Electric Co. · Jul 2006
GE LOGIQ P5 AND A5
K060993 · General Electric Co. · May 2006
GE VIVID 7 MODEL FC008XX, GE VIVID 7 MODEL FC009XX
K060542 · General Electric Co. · Mar 2006
GE VOLUSON I
K053435 · General Electric Co. · Dec 2005