Cleared Traditional

K141524 - NEURO-AUDIO

K141524 is an FDA 510(k) clearance for NEURO-AUDIO, manufactured by Teleemg, LLC USA. The device is a Class 2 Ear, Nose, Throat device with product code EWO cleared through the Traditional 510(k) pathway after a 276-day FDA review.

K141524 · Teleemg, LLC USA · Ear, Nose, Throat device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Mar 2015
Decision
276d
Days
Class 2
Risk

K141524 is an FDA 510(k) clearance for the NEURO-AUDIO. Classified as Audiometer (product code EWO), Class II - Special Controls.

Submitted by Teleemg, LLC USA (Salem, US). The FDA issued a Cleared decision on March 12, 2015 after a review of 276 days - an extended review cycle.

This device falls under the Ear, Nose, Throat FDA review panel, regulated under 21 CFR 874.1050 - the FDA ear, nose and throat 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 Ear, Nose, Throat review framework, consistent with the majority of Class II 510(k) submissions.

View all Teleemg, LLC USA devices

FDA 510(k) Submission Details - K141524

510(k) Number K141524 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received June 09, 2014
Decision Date March 12, 2015
Days to Decision 276 days
Submission Type Traditional
Review Panel Ear, Nose, Throat (EN)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
187d slower than avg
Panel avg: 89d · This submission: 276d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

EWO Device Classification - Class 2, Special Controls

Product Code EWO Audiometer
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 874.1050
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 Ear, Nose, Throat devices follow this clearance model.

Regulatory Peers - EWO Audiometer

All 55
Devices cleared under the same product code (EWO) and FDA review panel - the closest regulatory comparables to K141524.
Lyra
K191372 · Interacoustics A/S · Jul 2019
GSI Corti
K180287 · Grason-Stadler, Inc. · May 2018
Sera
K173567 · Interacoustics A/S · Feb 2018
AUDX PRO OTOACOUSTIC EMISSIONS MEASUREMENT SYSTEM
K122496 · Bio-Logic Systems Corp. · Nov 2012
SCOUT SPORT OTOACOUSTIC EMISSIONS MEASUREMENT SYSTEM
K121512 · Bio-Logic Systems Corp. · Jul 2012
COCHLEA-SCAN / COCHLEA-SCAN PLUS
K061744 · Bio-Logic Systems Corp. · Sep 2006