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

NICOLET AMP 6R11 SYSTEM

K Number: K871678 · Decision Jul 16, 1987
Classifications
1
FEI Numbers
25
Registration Numbers
25
Same Product Code
52
Applicant Total
26
Review Days
79

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Basic Information

Device Name
NICOLET AMP 6R11 SYSTEM
K Number
K871678
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
882.1835
Medical Specialty
Neurology
Decision
Substantially Equivalent
Applicant
Nicolet Biomedical Instruments
Date Received
April 28, 1987
Decision Date
July 16, 1987
Product Code
GWL
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
GWL Amplifier, Physiological Signal

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Other Clearances by Nicolet Biomedical Instruments

K Number Device Name
K880573 MODIFIED NICOLET VIKING SYSTEM
K873736 NICOLET DIGITAL TWO PIECE HEARING AID
K873964 NICOLET DISPOSABLE PRASS PROBE
K873535 NICOLET EXPERT SLEEP/WAKE ANALYSIS SYSTEM
K862592 PHOENIX SYSTEM SEVEN.
K851190 NYSTAGMOGRAPH EOG/ENG ANALYSES
K850108 EMG SURFACE, DIGITAL RING, BAR, GROUNDING, EEG
K850107 CONCENTRIC NEEDLE ELECTRODES-VARIOUS SIZES W/CONNE
K850259 ELECTROENCEPHALOGRAPH EEG
K843598 BRAIN FUNCTION MAPPING OPTION FOR PATHF
Search all 26 clearances from Nicolet Biomedical Instruments →