Cleared Traditional

K960330 - INSTATRAK

K960330 is an FDA 510(k) clearance for INSTATRAK, manufactured by Visualization Technology, Inc.. The device is a Class 2 Radiology device with product code LLZ cleared through the Traditional 510(k) pathway after a 75-day FDA review.

K960330 · Visualization Technology, Inc. · Radiology device
Download Printable Device Report (PDF) Official FDA 510(k) Summary (PDF)
Optimized for regulatory review, auditing and printing
Apr 1996
Decision
75d
Days
Class 2
Risk

K960330 is an FDA 510(k) clearance for the INSTATRAK. 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 Visualization Technology, Inc. (Woburn, US). The FDA issued a Cleared decision on April 8, 1996 after a review of 75 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 - K960330

510(k) Number K960330 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received January 24, 1996
Decision Date April 08, 1996
Days to Decision 75 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
32d faster than avg
Panel avg: 107d · This submission: 75d
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 2268
Devices cleared under the same product code (LLZ) and FDA review panel - the closest regulatory comparables to K960330.
ECHONET
K960946 · Lockheed Martin Communications Systems · May 1996
GE ADVANTAGE WINDOWS REVIEW WORKSTATION
K960613 · GE Medical Systems · Apr 1996
IMAGEFUSION
K960071 · Radionics Software Applications, Inc. · Apr 1996
KODAK CARDIOLOGY DIGITAL ARCHIVE & REVIEW SYSTEM
K960043 · Jamieson Film Co. · Mar 1996
DIGITAL IMAGING SYSTEM
K954159 · Camtronics, Ltd. · Mar 1996
PREVIEW SURGERY PLANNING SOFTWARE
K953616 · Medical Media Systems · Feb 1996
K960330 · INSTATRAK
Download PDF FDA Summary Visualization Technol…