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

THE SCREENER GSI 55 ABR SCREENER

K Number: K870030 · Decision Mar 13, 1987
Classifications
1
FEI Numbers
57
Registration Numbers
57
Same Product Code
75
Applicant Total
16
Review Days
67

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Basic Information

Device Name
THE SCREENER GSI 55 ABR SCREENER
K Number
K870030
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
882.1900
Medical Specialty
Neurology
Decision
Substantially Equivalent
Applicant
Grason-Stadler, Inc.
Date Received
January 5, 1987
Decision Date
March 13, 1987
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 Grason-Stadler, Inc.

K Number Device Name
K180287 GSI Corti
K172403 GSI Novus
K000097 GSI 2000 MIDDLE EAR ANALYZER
K974237 GSI 70 AUDIOPATH SCREENER
K970324 GSI SA60 DPOAE SYSTEM
K953684 GSI 61 CLINICAL AUDIOMETER
K951759 GSI 65 COMPUTERIZED AUDIOMETER
K902540 GSI 17 SCREENING AUDIOMETER
K890124 ILO88 OTODYNAMIC ANALYZER SCREENING AUDIOMETER
K863353 MIDDLE EAR ANALYZER (IMPEDANCE AUDIOMETER)
Search all 16 clearances from Grason-Stadler, Inc. →