Cleared Traditional

K131390 - JUSHA-M52C MEDICAL DISPLAY

K131390 is an FDA 510(k) clearance for JUSHA-M52C MEDICAL DISPLAY, manufactured by Nanjing Jusha Display Technology Co., Ltd.. The device is a Class 2 Radiology device with product code LLZ cleared through the Traditional 510(k) pathway after a 197-day FDA review.

K131390 · Nanjing Jusha Display Technology Co., Ltd. · Radiology device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Nov 2013
Decision
197d
Days
Class 2
Risk

K131390 is an FDA 510(k) clearance for the JUSHA-M52C MEDICAL DISPLAY. 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 Nanjing Jusha Display Technology Co., Ltd. (Guangzhou, Guangdong, CN). The FDA issued a Cleared decision on November 27, 2013 after a review of 197 days - an extended review 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 Nanjing Jusha Display Technology Co., Ltd. devices

FDA 510(k) Submission Details - K131390

510(k) Number K131390 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received May 14, 2013
Decision Date November 27, 2013
Days to Decision 197 days
Submission Type Traditional
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
90d slower than avg
Panel avg: 107d · This submission: 197d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

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 1190
Devices cleared under the same product code (LLZ) and FDA review panel - the closest regulatory comparables to K131390.
DYNACAD/PROSTATE INTERVENTIONAL (DYNALOC/PROSTATE)
K133030 · Invivo Corporation · Jan 2014
SYNGO.VIA WEB VIEWER
K130998 · Siemens AG Medical Solutions · Jan 2014
SIDEXIS 4
K132773 · Sirona Dental Systems GmbH · Dec 2013
MULTIVIEW
K132316 · Hologic, Inc. · Oct 2013
MAMMOGRAPHY VIEWER SMV658
K132188 · Fujifilm Medical System U.S.A., Inc. · Oct 2013
DYONICS PLAN HIP IMPINGEMENT PLANNING SYSTEM
K132636 · Smith & Nephew, Inc. · Oct 2013