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

DA VINCHI EEG AND EMG/EP SYSTEMS

K Number: K000963 · Decision Oct 20, 2000
Classifications
1
FEI Numbers
88
Registration Numbers
88
Same Product Code
138
Applicant Total
18
Review Days
210

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Basic Information

Device Name
DA VINCHI EEG AND EMG/EP SYSTEMS
K Number
K000963
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
882.1870
Medical Specialty
Neurology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Airsep Corp.
Date Received
March 24, 2000
Decision Date
October 20, 2000
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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K020324 LIFESTYLE OXYGEN CONCENTRATOR
K012037 HEALTHLIFE OXYGEN CONCENTRATOR MODEL AS009
K001579 IMPULSE SELECT
K001467 DA VINCHI EMG/EP ISA1004EP
K001013 MONET ACQUISITION SYSTEM FOR EEG AND POLYSOMNOGRAPHY
K992283 ARTISAN ACQUISITION SYSTEM FOR EEG AND POLYSOMNOGRAPHY
K983002 MYSTIQUE ULTRASONIC NEBULIZER
K960309 AIRSEP NEWLIFE DUAL SIX OXYGEN CONCENTRATOR (MODIFICATION)
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