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

MODIFIED NICOLET VIKING SYSTEM

K Number: K880573 · Decision Mar 22, 1988
Classifications
1
FEI Numbers
70
Registration Numbers
70
Same Product Code
74
Applicant Total
26
Review Days
41

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Basic Information

Device Name
MODIFIED NICOLET VIKING SYSTEM
K Number
K880573
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
890.1375
Medical Specialty
Physical Medicine
Decision
Substantially Equivalent
Applicant
Nicolet Biomedical Instruments
Date Received
February 10, 1988
Decision Date
March 22, 1988
Product Code
IKN
Advisory Committee
Physical Medicine
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
IKN Electromyograph, Diagnostic

Similar 510(k) Clearances

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Other Clearances by Nicolet Biomedical Instruments

K Number Device Name
K873736 NICOLET DIGITAL TWO PIECE HEARING AID
K873964 NICOLET DISPOSABLE PRASS PROBE
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 →