Cleared Traditional

K052904 - VIRTUAL MEDICAL SYSTEMS MODEL VT3000

K052904 is an FDA 510(k) clearance for VIRTUAL MEDICAL SYSTEMS MODEL VT3000, manufactured by Scientific Imaging, Inc.. The device is a Class 2 Neurology device with product code JXE cleared through the Traditional 510(k) pathway after a 13-day FDA review.

K052904 · Scientific Imaging, Inc. · Neurology device
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Oct 2005
Decision
13d
Days
Class 2
Risk

K052904 is an FDA 510(k) clearance for the VIRTUAL MEDICAL SYSTEMS MODEL VT3000. Classified as Device, Nerve Conduction Velocity Measurement (product code JXE), Class II - Special Controls.

Submitted by Scientific Imaging, Inc. (Woodstock, US). The FDA issued a Cleared decision on October 27, 2005 after a review of 13 days - a notably fast clearance cycle.

This device falls under the Neurology FDA review panel, regulated under 21 CFR 882.1550 - the FDA neurology device framework. The Traditional 510(k) pathway establishes clearance through substantial equivalence to a legally marketed predicate device, without requiring clinical trial data.

Device pattern: Fast-track predicate clearance. Standard predicate reliance. The short review cycle indicates strong predicate alignment - the FDA found sufficient equivalence without extended technical review.

View all Scientific Imaging, Inc. devices

FDA 510(k) Submission Details - K052904

510(k) Number K052904 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received October 14, 2005
Decision Date October 27, 2005
Days to Decision 13 days
Submission Type Traditional
Review Panel Neurology (NE)
Summary Statement
Third-party Review Yes - reviewed by an FDA-accredited third party
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
135d faster than avg
Panel avg: 148d · This submission: 13d
Pathway characteristics
Predicate-based equivalence. No clinical trials required. Third-party reviewed.

JXE Device Classification - Class 2, Special Controls

Product Code JXE Device, Nerve Conduction Velocity Measurement
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 882.1550
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 Neurology devices follow this clearance model.

Regulatory Consultant

Intertek Testing Services
NEIL E DEVINE

The regulatory consultant manages the 510(k) submission process on behalf of the applicant - coordinating technical documentation, predicate strategy and FDA communications. Identifying the consultant behind a submission is a key signal for competitive regulatory intelligence.

Regulatory Peers - JXE Device, Nerve Conduction Velocity Measurement

All 14
Devices cleared under the same product code (JXE) and FDA review panel - the closest regulatory comparables to K052904.
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