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

GN OTOMETRICS INSERT EARPHONES

K Number: K081234 · Decision Jul 14, 2008
Classifications
1
FEI Numbers
62
Registration Numbers
62
Same Product Code
234
Applicant Total
8
Review Days
74

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Basic Information

Device Name
GN OTOMETRICS INSERT EARPHONES
K Number
K081234
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
874.1050
Medical Specialty
Ear, Nose, Throat
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Gn Otometrics
Date Received
May 1, 2008
Decision Date
July 14, 2008
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

Other 510(k) clearances with the same product code (EWO), ordered by most recent decision date.

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Other Clearances by Gn Otometrics

K Number Device Name
K161707 Madsen Zodiac
K151504 ICS Impulse
K132957 MADSEN ACCUSCREEN TYPE 1077
K122550 ICS IMPULSE
K122028 AURICAL HIT
K122067 TYPE 1077 ACCUSCREEN
K092373 ICS CHARTR EP 200