Cleared Traditional

K864345 - NTE-2 THERMAL SENSITIVITY TESTER (FDA 510(k) Clearance)

Class I Neurology device.

K864345 · Sensortek, Inc. · Neurology device
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Jan 1987
Decision
86d
Days
Class 1
Risk

K864345 is an FDA 510(k) clearance for the NTE-2 THERMAL SENSITIVITY TESTER. Classified as Test, Temperature Discrimination (product code LQW), Class I - General Controls.

Submitted by Sensortek, Inc. (Clifton, US). The FDA issued a Cleared decision on January 29, 1987 after a review of 86 days - a notably fast clearance cycle.

This device falls under the Neurology FDA review panel, regulated under 21 CFR 882.1200 - 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 Sensortek, Inc. devices

Submission Details

510(k) Number K864345 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received November 04, 1986
Decision Date January 29, 1987
Days to Decision 86 days
Submission Type Traditional
Review Panel Neurology (NE)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
62d faster than avg
Panel avg: 148d · This submission: 86d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code LQW Test, Temperature Discrimination
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 882.1200
What this classification means

Class I devices are subject to general controls only and most are exempt from 510(k) premarket notification. They represent the lowest regulatory burden in the FDA device framework.