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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 K931975
Device Name AUDIOTECH MODEL DP
Applicant
MUSKOGEE REGIONAL HEARING AID LAB
2019 WEST BROADWAY
MUSKOGEE,  OK  74401
Applicant Contact DON LANGSTON
Correspondent
MUSKOGEE REGIONAL HEARING AID LAB
2019 WEST BROADWAY
MUSKOGEE,  OK  74401
Correspondent Contact DON LANGSTON
Regulation Number874.3300
Classification Product Code
ESD  
Date Received04/22/1993
Decision Date 06/22/1993
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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