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

DA VINCHI EMG/EP ISA1004EP

K Number: K001467 · Decision Aug 1, 2000
Classifications
1
FEI Numbers
37
Registration Numbers
37
Same Product Code
48
Applicant Total
18
Review Days
83

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Basic Information

Device Name
DA VINCHI EMG/EP ISA1004EP
K Number
K001467
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
882.1890
Medical Specialty
Neurology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Airsep Corp.
Date Received
May 10, 2000
Decision Date
August 1, 2000
Product Code
GWE
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
GWE Stimulator, Photic, Evoked Response

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K020324 LIFESTYLE OXYGEN CONCENTRATOR
K012037 HEALTHLIFE OXYGEN CONCENTRATOR MODEL AS009
K000963 DA VINCHI EEG AND EMG/EP SYSTEMS
K001579 IMPULSE SELECT
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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