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

IMMITTANCE METER, MODEL AE-105D/S

K Number: K905212 · Decision Feb 19, 1991
Classifications
1
FEI Numbers
14
Registration Numbers
14
Same Product Code
69
Applicant Total
20
Review Days
91

Basic Information

Device Name
IMMITTANCE METER, MODEL AE-105D/S
K Number
K905212
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
874.1090
Medical Specialty
Ear, Nose, Throat
Decision
Substantially Equivalent
Applicant
AMERICAN ELECTROMEDICS CORP.
Date Received
November 20, 1990
Decision Date
February 19, 1991
Product Code
ETY
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
ETY Tester, Auditory Impedance

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