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

STERILE SUBDERMAL NEEDLE ELECTRODES

K Number: K010019 · Decision Mar 19, 2001
Classifications
1
FEI Numbers
64
Registration Numbers
64
Same Product Code
52
Applicant Total
10
Review Days
76

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Basic Information

Device Name
STERILE SUBDERMAL NEEDLE ELECTRODES
K Number
K010019
Device Class
FDA class 2
Clearance Type
Abbreviated
Regulation Number
882.1350
Medical Specialty
Neurology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Nicolet Biomedical, Inc.
Date Received
January 2, 2001
Decision Date
March 19, 2001
Product Code
GXZ
Advisory Committee
Neurology
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
GXZ Electrode, Needle

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K011818 STERILE EMG ELECTRODES
K011823 BIOREHAB SYSTEM
K991054 BRAVO MULTI-MODALITY SYSTEM
K971331 SATELLITE
K950270 NMI SOFTWARE