Tool · 510(k)

510(k) Predicate Finder

Find potential predicate devices for your 510(k) submission. Enter a K-number to find all clearances with the same product code, a three-letter product code to browse clearances directly, or search by device name.

Product Code: EWO FDA class 2

Audiometer

Ear, Nose, Throat

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The audiometer is a diagnostic device used by audiologists and clinicians to measure a patient's hearing sensitivity across a range of frequencies and intensities, producing an audiogram that characterizes the type and degree of hearing loss. It is classified as FDA Class 2, indicating moderate risk and requiring special controls. The product code is EWO, regulated under 21 CFR 874.1050 in the Ear, Nose, Throat specialty. No implant, life-sustaining, GMP-exempt, or third-party review designations apply.

510(k) Clearances

50+ matches
K Number
Device Name
OtoNova/OtoNova Pro
Otoport Pro
hearOAE
Sentiero, AuDX, AuDX PRO, Sentiero Desktop, AuDX PRO Flex, Sentiero Advanced, NavPRO ONE
Lyra
GSI Corti
Sera
GSI Novus
Easyscreen
iHearTest
ER36 Series OAE Test System
NEURO-AUDIO
Otoport OAE +ABR Advance, Otoport OAE+ABR DP+TE, Otoport OAE+ABR Screener-Otocheck OAE+ABR, Otocheck OAE+ABR LE, Otocheck ABR Screener-Otodynamics ABR Upgrade Kit
SENTIERO
TITAN
OTOSTAT DPOAE + MEPA MEASUREMENT SYSTEM
AUDX PRO OTOACOUSTIC EMISSIONS MEASUREMENT SYSTEM
SCOUT SPORT OTOACOUSTIC EMISSIONS MEASUREMENT SYSTEM
EARLOGIC OAE TESTER
A BAER WITH ABAER I/O FUNCTION
AUDX OTOACOUSTIC EMISSIONS MEASUREMENT SYSTEM WITH AUDX I/O FUNCTION
ER35 ERO-SCAN PRO HEARING TEST SYSTEM
ACAM 5 AUDIOMETER SYSTEM
CLARUJUST
MA61, MA62, MA63 FAMILY OF PORTABLE AUDIOMETERS
ENTOMED SCREENING AUDIOMETER, MODEL SA201,SA202, ENTOMED DIAGNOSTIC AUDIOMETER MODEL SA203,SA204
EP15 SOFTWARE MODULE, EP25 SOFTWARE MODULE
GN OTOMETRICS INSERT EARPHONES
OTODYNAMICS OTOPORT
ER35 ERO-SCAN PRO HEARING TEST SYSTEM
MA 55 MAESTRO
OTOGRAM, CA3350
HEARID+TE TRANSIENT-EVOKED OTOACOUSTIC EMISSIONS ANALYZER
COCHLEA-SCAN / COCHLEA-SCAN PLUS
PILOT TEST OR DETECTIVE AUDIOMETERS
MODEL MI 44 TYMPANOMETER
DPOAE20 , ECLIPSE
HEARID WIDEBAND MIDDLE EAR POWER ANALYZER
ECLIPSE (CABINET NAME), TEOAE25, EP15, OR THE COMBINATION OF SYSTEMS.
AFFINITY (CABINET NAME), AC440, HIT440, OR THE COMBINATION OF SYSTEMS
VIVO 200 DPS VIVOSCAN VERSION 2.0 OAE AUDIOMETER
AUDIOMETER, OTOACOUSTIC EMISSION, AUDITORY BRANSTEM RESPONSE ACCESS
ICS MEDICAL CHARTR EP WITH ASSR AND CHARTR OAE SYSTEMS
BIO-LOGIC INSERT EARPHONES
TEOAE25
AUDIOSCREENER OAE+ABR
SMARTTROAE
BIO-LOGIC ABAER CUB WITH INTEGRATED OAE & ABR FUNCTIONS
GSI AUDERA
VIVO 200 DPS VIVOSCAN

What is a Predicate Device?

A predicate device is a legally marketed device that a new 510(k) applicant uses to demonstrate substantial equivalence. The FDA's 510(k) pathway requires manufacturers to show that their device has the same intended use and similar technological characteristics as one or more predicate devices already cleared for commercial distribution.

Finding the right predicate is a critical step in 510(k) strategy. Manufacturers typically search for cleared devices with the same FDA product code, which groups devices by their intended use and regulatory classification. This tool helps you identify potential predicates by browsing all clearances within a product code.

Note that predicate devices must be legally marketed — they cannot be devices that were cleared but never commercialized, or devices subject to a mandatory recall. The determination of substantial equivalence considers intended use, technological characteristics, and performance data.

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