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

VARIOUS ELECTRODES

K Number: K941928 · Decision Feb 3, 1995
Classifications
1
FEI Numbers
15
Registration Numbers
15
Same Product Code
58
Applicant Total
45
Review Days
289

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Basic Information

Device Name
VARIOUS ELECTRODES
K Number
K941928
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
882.1460
Medical Specialty
Neurology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Bio-Logic Systems Corp.
Date Received
April 20, 1994
Decision Date
February 3, 1995
Product Code
GWN
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
GWN Nystagmograph

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Other Clearances by Bio-Logic Systems Corp.

K Number Device Name
K122496 AUDX PRO OTOACOUSTIC EMISSIONS MEASUREMENT SYSTEM
K121512 SCOUT SPORT OTOACOUSTIC EMISSIONS MEASUREMENT SYSTEM
K073626 BIO-LOGIC MASTER II EVOKED RESPONSE SYSTEM
K061744 COCHLEA-SCAN / COCHLEA-SCAN PLUS
K052066 CEEGRAPH/SLEEPSCAN NETLINK TRAVELER
K031352 BIO-LOGIC INSERT EARPHONES
K030907 STACKED ABR FOR NAVIGATOR PRO
K031009 MODIFICATION TO BIO-LOGIC EVOKED POTENTIAL (EP) SYSTEM
K021895 BIO-LOGIC MASTER EVOKED RESPONSE SYSTEM
K021801 BIO-LOGIC ABAER CUB WITH INTEGRATED OAE & ABR FUNCTIONS
Search all 45 clearances from Bio-Logic Systems Corp. →