Cleared Traditional

K131290 - IQ TECHNOLOGIES

K131290 is an FDA 510(k) clearance for IQ TECHNOLOGIES, manufactured by Iq Technologies, Inc.. The device is a Class 2 Neurology device with product code NUH cleared through the Traditional 510(k) pathway after a 457-day FDA review.

K131290 · Iq Technologies, Inc. · Neurology device
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Aug 2014
Decision
457d
Days
Class 2
Risk

K131290 is an FDA 510(k) clearance for the IQ TECHNOLOGIES. Classified as Stimulator, Nerve, Transcutaneous, Over-the-counter (product code NUH), Class II - Special Controls.

Submitted by Iq Technologies, Inc. (Las Vegas, US). The FDA issued a Cleared decision on August 6, 2014 after a review of 457 days - an unusually long review period, suggesting complex equivalence evaluation.

This device falls under the Neurology FDA review panel, regulated under 21 CFR 882.5890 - 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: High-complexity regulatory submission. Elevated predicate reliance profile. The extended review timeline suggests the FDA required additional documentation before confirming substantial equivalence - a pattern common in complex or first-of-kind Neurology submissions.

View all Iq Technologies, Inc. devices

FDA 510(k) Submission Details - K131290

510(k) Number K131290 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received May 06, 2013
Decision Date August 06, 2014
Days to Decision 457 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
309d slower than avg
Panel avg: 148d · This submission: 457d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

NUH Device Classification - Class 2, Special Controls

Product Code NUH Stimulator, Nerve, Transcutaneous, Over-the-counter
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 882.5890
Definition Temporary Relief Of Pain Due To Sore/aching Muscles
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 - NUH Stimulator, Nerve, Transcutaneous, Over-the-counter

All 163
Devices cleared under the same product code (NUH) and FDA review panel - the closest regulatory comparables to K131290.
Transcutaneous Electrical Nerve Stimulators (TENS)
K150043 · Andon Health Co, Ltd. · Aug 2015
MAXPOWER RELIEF
K141978 · Omron Healthcare, Inc. · Dec 2014
OTC COMBO TENS/EMS SYSTEM
K141299 · Well-Life Healthcare Limited · Nov 2014
ASCEND
K140333 · Neurometrix, Inc. · Jul 2014
HIVOX ELECTRIC STIMULATOR OTC TENS
K140650 · Hivox Biotek, Inc. · Jun 2014
OTC PATCH
K133723 · Well-Life Healthcare Limited · Jan 2014