Cleared Traditional

K062905 - NIO FUSION 4MP

Also marketed or referenced as:
MDNC 4130

K062905 is an FDA 510(k) clearance for NIO FUSION 4MP, manufactured by Barcoview. The device is a Class 2 Radiology device with product code LLZ cleared through the Traditional 510(k) pathway after a 93-day FDA review.

K062905 · Barcoview · Radiology device
Download Printable Device Report (PDF) Official FDA 510(k) Summary (PDF)
Optimized for regulatory review, auditing and printing
Dec 2006
Decision
93d
Days
Class 2
Risk

K062905 is an FDA 510(k) clearance for the NIO FUSION 4MP. 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 Barcoview (8500 Kortrijk, BE). The FDA issued a Cleared decision on December 29, 2006 after a review of 93 days - within the typical 510(k) review window.

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.

FDA 510(k) Submission Details - K062905

510(k) Number K062905 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received September 27, 2006
Decision Date December 29, 2006
Days to Decision 93 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
14d faster than avg
Panel avg: 107d · This submission: 93d
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 2241
Devices cleared under the same product code (LLZ) and FDA review panel - the closest regulatory comparables to K062905.
SYNGO MI APPLICATIONS 2007A
K063826 · Siemens Medical Solutions USA, Inc. · Jan 2007
AYCAN WORKSTATION OSIRIX
K063470 · Aycan Digitalsysteme GmbH · Jan 2007
PHILIPS XD-S DIRECT RADIOGRAPHY WORKSTATION/PACKAGE
K063781 · Philips Medical Systems North America Co. · Jan 2007
CENTRICITY RADIOLOGY RA600, CARDIOLOGY CA1000 AND DIGITAL HARDCOPY
K063628 · Ge Healthcare Integrated IT Solutions · Dec 2006
2MP MEDICAL COLOR REFERENCE DISPLAY, MODEL MDC2130-2HC
K063579 · Chi Lin Technology Co., Ltd. · Dec 2006
MEDWEB ADVANCED 3D WEB PACS
K063221 · Nexsys Electronics, Inc. · Dec 2006