FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

AE1162 CLINICAL/DIAGNOSTIC AUDIOMETER

K Number: K881760 · Decision Jun 10, 1988
Classifications
1
FEI Numbers
62
Registration Numbers
62
Same Product Code
234
Applicant Total
20
Review Days
46

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Basic Information

Device Name
AE1162 CLINICAL/DIAGNOSTIC AUDIOMETER
K Number
K881760
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
874.1050
Medical Specialty
Ear, Nose, Throat
Decision
Substantially Equivalent
Applicant
American Electromedics Corp.
Date Received
April 25, 1988
Decision Date
June 10, 1988
Product Code
EWO
Advisory Committee
Ear, Nose, Throat
Review Advisory Committee
EN
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
EWO Audiometer

Similar 510(k) Clearances

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Other Clearances by American Electromedics Corp.

K Number Device Name
K983051 AMERICAN ELECTROMEDICS RACE CA TYMPANOMETER/AUDIOMETER WITH INTEGRAL PRINTER
K983049 AMERICAN ELECTROMEDICS QUIK TYMP 1 (QT1) TYMPANOMETER WITH INTERGRAL PRINTER
K983046 AMERICAN ELECTROMEDICS RACE CAR TYMPANOMETER W/INTEGRAL PRINTER
K983048 AMERICAN ELECTROMEDICS QUIK TYMP 2 (QT2) TYMPANOMETER/AUDIOMETER WITH INTEGRAL PRINTER
K972221 K 15 AUDIOMETER
K970279 RACE CAR TYMPANOMETER WITH AUDIOMETER(AE-RCAUD I/QUIK TYMP 1(AE-QUIK 1)/QUICK TYMP 2(AE-QUIK 2)
K955289 RACE CAR TYMPANOMETER
K951527 THE PILOT AUDIOMETER
K930164 THE AUTOMATIC IMPEDANCE METER,MODEL AE-208D/S
K924933 AE-206 TYMPNOMWRWE(R) AUDIOMETER
Search all 20 clearances from American Electromedics Corp. →