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

MODIFCATION TO: NUVASIVE NEUROVISION EMG ENDOTRACHEAL TUBE

K Number: K094054 · Decision May 14, 2010
Classifications
1
FEI Numbers
88
Registration Numbers
88
Same Product Code
138
Applicant Total
91
Review Days
134

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Basic Information

Device Name
MODIFCATION TO: NUVASIVE NEUROVISION EMG ENDOTRACHEAL TUBE
K Number
K094054
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
882.1870
Medical Specialty
Neurology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Nuvasive, Inc.
Date Received
December 31, 2009
Decision Date
May 14, 2010
Product Code
GWF
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
GWF Stimulator, Electrical, Evoked Response

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