FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

K-AMP 16, HI-BAND K-AMP, ULTRA COMPRESSION & HEARING PROTECTION/HEARING INSTRUMENT

K Number: K954038 · Decision Sep 18, 1995
Classifications
1
FEI Numbers
117
Registration Numbers
117
Same Product Code
1366
Applicant Total
24
Review Days
21

Basic Information

Device Name
K-AMP 16, HI-BAND K-AMP, ULTRA COMPRESSION & HEARING PROTECTION/HEARING INSTRUMENT
K Number
K954038
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
874.3300
Medical Specialty
Ear, Nose, Throat
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
ARGOSY ELECTRONICS
Date Received
August 28, 1995
Decision Date
September 18, 1995
Product Code
ESD
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
ESD Hearing Aid, Air-Conduction, Prescription

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K952455 IMPROVED MANHATTAN II
K952453 INPUT COMPRSSION LIMITER WITH ACTIVE TONE CONTROL
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