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

NICOLET NYSTAR PLUS SYSTEM

K Number: K884294 · Decision Nov 23, 1988
Classifications
1
FEI Numbers
15
Registration Numbers
15
Same Product Code
58
Applicant Total
13
Review Days
42

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Basic Information

Device Name
NICOLET NYSTAR PLUS SYSTEM
K Number
K884294
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
882.1460
Medical Specialty
Neurology
Decision
Substantially Equivalent
Applicant
Nicolet Instrument Corp.
Date Received
October 12, 1988
Decision Date
November 23, 1988
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 Nicolet Instrument Corp.

K Number Device Name
K921138 NICOLET ULTRASOM ACQUISITION STATION
K923315 NICOLET ARK SYSTEM
K921927 NICOLET VOYAGEUR
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
Search all 13 clearances from Nicolet Instrument Corp. →