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

HEARLAB ACA

K Number: K123701 · Decision Apr 5, 2013
Classifications
1
FEI Numbers
57
Registration Numbers
57
Same Product Code
75
Applicant Total
13
Review Days
123

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Basic Information

Device Name
HEARLAB ACA
K Number
K123701
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
882.1900
Medical Specialty
Neurology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Frye Electronics, Inc.
Date Received
December 3, 2012
Decision Date
April 5, 2013
Product Code
GWJ
Advisory Committee
Neurology
Review Advisory Committee
NE
Third Party
N

Classifications

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

Product Code Device Name
GWJ Stimulator, Auditory, Evoked Response

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Other Clearances by Frye Electronics, Inc.

K Number Device Name
K093006 FONIX ,MODEL 8000
K022510 FONIX, MODEL 7000
K980377 FONIX FP35 HEARING AID ANALYZER
K935400 FONIX 3500 HEARING AID ANALYZER
K913221 TYPE FA10 AUDIOMETER
K895383 TYPE FP40 DIGITAL HEARING AID ANALYZER
K872242 TYPE 6400 REAL EAR HEARING AID ANALYZER
K861571 TYPE 6500 HEARING AID ANALYZER
K850918 TYPE FP30 DIGITAL HEARING AID ANALYZER
K833883 DIGITAL AUDIOMETER/HEARING AID 3100
Search all 13 clearances from Frye Electronics, Inc. →