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

NICOLET VOYAGEUR

K Number: K921927 · Decision Nov 5, 1992
Classifications
1
FEI Numbers
96
Registration Numbers
96
Same Product Code
188
Applicant Total
13
Review Days
195

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Basic Information

Device Name
NICOLET VOYAGEUR
K Number
K921927
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
882.1400
Medical Specialty
Neurology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Nicolet Instrument Corp.
Date Received
April 24, 1992
Decision Date
November 5, 1992
Product Code
GWQ
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
GWQ Full-Montage Standard Electroencephalograph

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (GWQ), ordered by most recent decision date.

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Other Clearances by Nicolet Instrument Corp.

K Number Device Name
K921138 NICOLET ULTRASOM ACQUISITION STATION
K923315 NICOLET ARK SYSTEM
K915652 NICOLET PORATBLE SPIRIT SYSTEM
K905632 NICOLET MAPLELEAF SYSTEM
K897154 NICOLET DBTE HEARING AID: DIGITAL & PROGRAMMABLE
K894629 NICOLET BEAM II SYSTEM
K896477 NICOLET REAL EAR ANALYZER
K883781 NICOLET NEUROPORT/ACE SYSTEM
K890495 NICOLET VIKING II SYSTEM
K884294 NICOLET NYSTAR PLUS SYSTEM
Search all 13 clearances from Nicolet Instrument Corp. →