Cleared Traditional

K062062 - VOYAGER PACS SYSTEM

K062062 is an FDA 510(k) clearance for VOYAGER PACS SYSTEM, manufactured by Voyager Imaging. The device is a Class 2 Radiology device with product code LLZ cleared through the Traditional 510(k) pathway after a 53-day FDA review.

K062062 · Voyager Imaging · Radiology device
Download Printable Device Report (PDF) Official FDA 510(k) Summary (PDF)
Optimized for regulatory review, auditing and printing
Sep 2006
Decision
53d
Days
Class 2
Risk

K062062 is an FDA 510(k) clearance for the VOYAGER PACS SYSTEM. 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 Voyager Imaging (Denton, US). The FDA issued a Cleared decision on September 11, 2006 after a review of 53 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.

FDA 510(k) Submission Details - K062062

510(k) Number K062062 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received July 20, 2006
Decision Date September 11, 2006
Days to Decision 53 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
54d faster than avg
Panel avg: 107d · This submission: 53d
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 2281
Devices cleared under the same product code (LLZ) and FDA review panel - the closest regulatory comparables to K062062.
IQ-SYSTEM PACS SYSTEM
K062488 · Image Information Systems, Ltd. · Sep 2006
GENTLE COLON (REVISION 2.0)
K061532 · Rendoscopy, Inc. · Sep 2006
CONNECT IMAGING PACS
K061972 · Connect Imaging, Inc. · Sep 2006
CTC WORKSTATION, MODEL 2200
K062229 · Medical Diagnostic Technologies, Inc. · Sep 2006
ART LAB SOFTWARE
K061961 · Pie Medical · Sep 2006
XCELERA
K061995 · Philips Medical Systems North America Co. · Sep 2006
K062062 · VOYAGER PACS SYSTEM
Download PDF FDA Summary Voyager Imaging