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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Masker, Tinnitus
510(k) Number K791142
Device Name HEARING AID, MODEL MA-1
Applicant
STARKEY LABORATORIES, INC.
803 N. Front St. Suite 3
McHenry,  IL  60050
Correspondent
STARKEY LABORATORIES, INC.
803 N. Front St. Suite 3
McHenry,  IL  60050
Regulation Number874.3400
Classification Product Code
KLW  
Date Received06/18/1979
Decision Date 09/28/1979
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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