Nicolet Biomedical Instruments is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Nicolet Biomedical Instruments - FDA 510(k) Cleared Devices
26
Total
26
Cleared
0
Denied
Nicolet Biomedical Instruments has 26 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 26 cleared submissions from 1977 to 1988. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Nicolet Biomedical Instruments Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Nicolet Biomedical Instruments
26 devices
Cleared
Mar 22, 1988
MODIFIED NICOLET VIKING SYSTEM
Neurology
41d
Cleared
Dec 08, 1987
NICOLET DIGITAL TWO PIECE HEARING AID
Ear, Nose, Throat
84d
Cleared
Nov 20, 1987
NICOLET DISPOSABLE PRASS PROBE
Ear, Nose, Throat
52d
Cleared
Oct 26, 1987
NICOLET EXPERT SLEEP/WAKE ANALYSIS SYSTEM
Neurology
55d
Cleared
Jul 16, 1987
NICOLET AMP 6R11 SYSTEM
Neurology
79d
Cleared
Sep 16, 1986
PHOENIX SYSTEM SEVEN.
Ear, Nose, Throat
70d
Cleared
Nov 27, 1985
NYSTAGMOGRAPH EOG/ENG ANALYSES
Neurology
246d
Cleared
Apr 11, 1985
BRAIN FUNCTION MAPPING OPTION FOR PATHF
Neurology
211d
Cleared
Apr 11, 1985
CONCENTRIC NEEDLE ELECTRODES-VARIOUS SIZES W/CONNE
Neurology
91d
Cleared
Apr 11, 1985
EMG SURFACE, DIGITAL RING, BAR, GROUNDING, EEG
Neurology
91d
Cleared
Apr 11, 1985
ELECTROENCEPHALOGRAPH EEG
Neurology
79d
Cleared
Aug 03, 1984
NICOLET VIKING
Neurology
7d