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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 K911708
Device Name MODEL E-50, IN-THE-EAR HEARING AID
Applicant
ELECTONE, INC.
1124 FLORIDA CENTRAL PKWY.
LONGWOOD,  FL  32750
Applicant Contact JIM NEE
Correspondent
ELECTONE, INC.
1124 FLORIDA CENTRAL PKWY.
LONGWOOD,  FL  32750
Correspondent Contact JIM NEE
Regulation Number874.3300
Classification Product Code
ESD  
Date Received04/16/1991
Decision Date 05/17/1991
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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