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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 K953921
Device Name PHONAK 9900 CIC
Applicant
PHONAK, INC.
850 E. DIEHL RD.
P.O. BOX 3017
NAPERVILLE,  IL  60566
Applicant Contact BILL LESIECKI
Correspondent
PHONAK, INC.
850 E. DIEHL RD.
P.O. BOX 3017
NAPERVILLE,  IL  60566
Correspondent Contact BILL LESIECKI
Regulation Number874.3300
Classification Product Code
ESD  
Date Received08/21/1995
Decision Date 09/18/1995
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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