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

EVOKED POTENTIAL SYS

K Number: K842543 · Decision Nov 29, 1984
Classifications
1
FEI Numbers
88
Registration Numbers
88
Same Product Code
138
Applicant Total
45
Review Days
150

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Basic Information

Device Name
EVOKED POTENTIAL SYS
K Number
K842543
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
882.1870
Medical Specialty
Neurology
Decision
Substantially Equivalent
Applicant
Bio-Logic Systems Corp.
Date Received
July 2, 1984
Decision Date
November 29, 1984
Product Code
GWF
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
GWF Stimulator, Electrical, Evoked Response

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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
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