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FDA 510(k) Application Details - K955879
Device Classification Name
Hearing Aid, Air Conduction
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510(K) Number
K955879
Device Name
Hearing Aid, Air Conduction
Applicant
WIDEX HEARING AID CO., INC.
35-53 24TH ST.
LONG ISLAND CITY, NY 11106 US
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Contact
RON MELTSNER
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Regulation Number
874.3300
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Classification Product Code
ESD
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Date Received
12/28/1995
Decision Date
02/27/1996
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
EN - Ear, Nose, & Throat
Review Advisory Committee
EN - Ear, Nose, & Throat
Statement / Summary / Purged Status
Statement
Type
Traditional
Reviewed By Third Party
N
Expedited Review
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