Cleared Traditional

K102166 - ELECTRO INTERSTITIAL SCAN

K102166 is an FDA 510(k) clearance for ELECTRO INTERSTITIAL SCAN, manufactured by Ld Technology, LLC. The device is a Class 2 Neurology device with product code GZO cleared through the Traditional 510(k) pathway after a 130-day FDA review.

K102166 · Ld Technology, LLC · Neurology device
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Dec 2010
Decision
130d
Days
Class 2
Risk

K102166 is an FDA 510(k) clearance for the ELECTRO INTERSTITIAL SCAN. Classified as Device, Galvanic Skin Response Measurement (product code GZO), Class II - Special Controls.

Submitted by Ld Technology, LLC (Miami, US). The FDA issued a Cleared decision on December 10, 2010 after a review of 130 days - within the typical 510(k) review window.

This device falls under the Neurology FDA review panel, regulated under 21 CFR 882.1540 - 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: Standard predicate-based submission. Standard predicate reliance. This clearance follows a standard predicate-based equivalence path within the Neurology review framework, consistent with the majority of Class II 510(k) submissions.

View all Ld Technology, LLC devices

FDA 510(k) Submission Details - K102166

510(k) Number K102166 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received August 02, 2010
Decision Date December 10, 2010
Days to Decision 130 days
Submission Type Traditional
Review Panel Neurology (NE)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
18d faster than avg
Panel avg: 148d · This submission: 130d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

GZO Device Classification - Class 2, Special Controls

Product Code GZO Device, Galvanic Skin Response Measurement
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 882.1540
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 Peers - GZO Device, Galvanic Skin Response Measurement

All 9
Devices cleared under the same product code (GZO) and FDA review panel - the closest regulatory comparables to K102166.
SUDOSCAN
K141872 · Impeto Medical, Inc. · Nov 2014
SUDO PATH
K131568 · Ld Technology, LLC · Jun 2013
ZYTO HAND CRADLE
K111308 · Zyto Technologies, Inc. · Aug 2011
MSAS PROFESSIONAL
K993824 · Biomeridian, Int. · Jan 2000
EIM-107 PREP-CHECK
K993202 · General Devices · Dec 1999
PHAZX VLD-100
K992129 · Phazx Systems, Inc. · Sep 1999