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

SMARTOAE

K Number: K964426 · Decision Feb 3, 1997
Classifications
1
FEI Numbers
62
Registration Numbers
62
Same Product Code
234
Applicant Total
13
Review Days
90

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Basic Information

Device Name
SMARTOAE
K Number
K964426
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
874.1050
Medical Specialty
Ear, Nose, Throat
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Intelligent Hearing Systems
Date Received
November 5, 1996
Decision Date
February 3, 1997
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 Intelligent Hearing Systems

K Number Device Name
K163326 SmartEP
K090579 SMARTSCREENER-PLUS2
K073384 SMART COUPLER, MODEL M015401
K070608 SMARTEP, MODEL M010000
K063402 WICK ELECTRODE, MODEL M019260
K061443 SMART USBLITE, MODEL M011120
K052060 OPTI-AMP DC-POWERED
K031051 SMARTEP-ASSR, MODEL M811007
K023859 SMARTTROAE
K925648 SMART-SCREENER (AUDITORY)
Search all 13 clearances from Intelligent Hearing Systems →