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

PHOENIX SYSTEM SEVEN.

K Number: K862592 · Decision Sep 16, 1986
Classifications
1
FEI Numbers
62
Registration Numbers
62
Same Product Code
234
Applicant Total
26
Review Days
70

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Basic Information

Device Name
PHOENIX SYSTEM SEVEN.
K Number
K862592
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
874.1050
Medical Specialty
Ear, Nose, Throat
Decision
Substantially Equivalent
Applicant
Nicolet Biomedical Instruments
Date Received
July 8, 1986
Decision Date
September 16, 1986
Product Code
EWO
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
EWO Audiometer

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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
K871678 NICOLET AMP 6R11 SYSTEM
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 →