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

NICOLET ULTRASOM ACQUISITION STATION

K Number: K921138 · Decision May 14, 1993
Classifications
1
FEI Numbers
97
Registration Numbers
97
Same Product Code
186
Applicant Total
13
Review Days
430

Basic Information

Device Name
NICOLET ULTRASOM ACQUISITION STATION
K Number
K921138
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
March 10, 1992
Decision Date
May 14, 1993
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

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K Number Device Name
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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
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