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

NICOLET DISPOSABLE PRASS PROBE

K Number: K873964 · Decision Nov 20, 1987
Classifications
1
FEI Numbers
140
Registration Numbers
140
Same Product Code
96
Applicant Total
26
Review Days
52

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Basic Information

Device Name
NICOLET DISPOSABLE PRASS PROBE
K Number
K873964
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
874.1820
Medical Specialty
Ear, Nose, Throat
Decision
Substantially Equivalent
Applicant
Nicolet Biomedical Instruments
Date Received
September 29, 1987
Decision Date
November 20, 1987
Product Code
ETN
Advisory Committee
Ear, Nose, Throat
Review Advisory Committee
EN
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
ETN Stimulator, Nerve

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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
K873535 NICOLET EXPERT SLEEP/WAKE ANALYSIS SYSTEM
K871678 NICOLET AMP 6R11 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 →