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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name hearing aid, air-conduction, prescription
510(k) Number K963604
Device Name DYNAMIC EQ II - 2 CHANNEL WIDE DYNAMIC RANGE COMPRESSION
Applicant
MIDWEST CITY HEARING AID CENTER
1401 SOUTH MIDWEST BLVD.
MIDWEST CITY,  OK  73110
Applicant Contact FRANKLIN D CARTER
Correspondent
MIDWEST CITY HEARING AID CENTER
1401 SOUTH MIDWEST BLVD.
MIDWEST CITY,  OK  73110
Correspondent Contact FRANKLIN D CARTER
Regulation Number874.3300
Classification Product Code
ESD  
Date Received09/09/1996
Decision Date 09/27/1996
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Ear Nose & Throat
510k Review Panel Ear Nose & Throat
Type Traditional
Reviewed by Third Party No
Combination Product No
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