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Nicolet Biomedical Instruments

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
26
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K880573MODIFIED NICOLET VIKING SYSTEMMarch 22, 1988
K873736NICOLET DIGITAL TWO PIECE HEARING AIDDecember 8, 1987
K873964NICOLET DISPOSABLE PRASS PROBENovember 20, 1987
K873535NICOLET EXPERT SLEEP/WAKE ANALYSIS SYSTEMOctober 26, 1987
K871678NICOLET AMP 6R11 SYSTEMJuly 16, 1987
K862592PHOENIX SYSTEM SEVEN.September 16, 1986
K851190NYSTAGMOGRAPH EOG/ENG ANALYSESNovember 27, 1985
K843598BRAIN FUNCTION MAPPING OPTION FOR PATHFApril 11, 1985
K850259ELECTROENCEPHALOGRAPH EEGApril 11, 1985
K850108EMG SURFACE, DIGITAL RING, BAR, GROUNDING, EEGApril 11, 1985
K850107CONCENTRIC NEEDLE ELECTRODES-VARIOUS SIZES W/CONNEApril 11, 1985
K842956NICOLET VIKINGAugust 3, 1984
K842612COMPACT AUDITORYJuly 20, 1984
K842611CA2000July 20, 1984
K842613COMPACT VISUALJuly 20, 1984
K831896COMPACT FOURJuly 28, 1983
K830702NICOLET EMG SATELLITEJuly 12, 1983
K830579MULTI-SIGNAL AUDITORY STIMULATOR SM700March 8, 1983
K822215NIC OPTRONICS CS-2000August 31, 1982
K813399ERG-JET ELECTRODEJanuary 22, 1982