FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

HEARING AID ANALYSIS SYSTEM

K Number: K853271 · Decision Jan 16, 1986
Classifications
1
FEI Numbers
15
Registration Numbers
15
Same Product Code
45
Applicant Total
21
Review Days
164

Basic Information

Device Name
HEARING AID ANALYSIS SYSTEM
K Number
K853271
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
874.3310
Medical Specialty
Ear, Nose, Throat
Decision
Substantially Equivalent
Applicant
ROBERT BOSCH CORP.
Date Received
August 5, 1985
Decision Date
January 16, 1986
Product Code
ETW
Advisory Committee
Ear, Nose, Throat
Review Advisory Committee
EN
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
ETW Calibrator, Hearing Aid / Earphone And Analysis Systems

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K853541 SP 4
K853154 HV-4
K851485 DEFI 502
K840717 ECS 502
K851937 SONOMED 4
K850188 BOSCH IN THE EAR HEARING AID SUPERSTAR
K850186 POST AURICULAR HEARING AIDS STAR 33PP, 44,55F &
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