Cleared Traditional

K122843 - MD211G3 21.3 DIAGNOSTIC IMAGING LCD MONITOR

K122843 is an FDA 510(k) clearance for MD211G3 21.3 DIAGNOSTIC IMAGING LCD MONITOR, manufactured by Prodigy Technology Consultant Co., Ltd.. The device is a Class 2 Radiology device with product code LLZ cleared through the Traditional 510(k) pathway after a 18-day FDA review.

K122843 · Prodigy Technology Consultant Co., Ltd. · Radiology device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Oct 2012
Decision
18d
Days
Class 2
Risk

K122843 is an FDA 510(k) clearance for the MD211G3 21.3 DIAGNOSTIC IMAGING LCD MONITOR. Classified as System, Image Processing, Radiological within the LLZ classification (a category encompassing advanced image processing and PACS-adjacent software), Class II - Special Controls.

Submitted by Prodigy Technology Consultant Co., Ltd. (Taipei, TW). The FDA issued a Cleared decision on October 5, 2012 after a review of 18 days - a notably fast clearance cycle.

This device falls under the Radiology FDA review panel, regulated under 21 CFR 892.2050 - 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: Incremental AI imaging tool. Moderate equivalence dependency. Overall, this clearance reflects a predicate-aligned approval typical of modern AI radiology extensions - not a novel clinical breakthrough, but a validated iteration within an established regulatory category.

View all Prodigy Technology Consultant Co., Ltd. devices

FDA 510(k) Submission Details - K122843

510(k) Number K122843 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received September 17, 2012
Decision Date October 05, 2012
Days to Decision 18 days
Submission Type Traditional
Review Panel Radiology (RA)
Summary Summary PDF
Third-party Review Yes - reviewed by an FDA-accredited third party
Regulatory Context
Review time vs. panel average
89d faster than avg
Panel avg: 107d · This submission: 18d
Pathway characteristics
Predicate-based equivalence. No clinical trials required. Third-party reviewed.

LLZ Device Classification - Class 2, Special Controls

Product Code LLZ System, Image Processing, Radiological
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 892.2050
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 - LLZ System, Image Processing, Radiological

All 1269
Devices cleared under the same product code (LLZ) and FDA review panel - the closest regulatory comparables to K122843.
IMAGE-COM 5.0
K122289 · Tomtec Imaging Systems GmbH · Oct 2012
CARESTREAM VUE PACS
K122523 · Carestream Health, Inc. · Oct 2012
ULTRAEXTEND FX, ULTRASOUND WORKSTATION PACKAGE
K121076 · Toshiba America Medical Systems, In.C · Oct 2012
ORTHOCAD SOFTWARE OPTION
K120288 · Esaote, S.P.A. · Sep 2012
VITREAVIEW
K122136 · Vital Images, Inc. · Sep 2012
MR VESSELLQ XPRESS
K122164 · GE Medical Systems SCS · Sep 2012