AKUPORT M1

Device, Galvanic Skin Response Measurement

VIBRANT HEALTH

The following data is part of a premarket notification filed by Vibrant Health with the FDA for Akuport M1.

Pre-market Notification Details

Device IDK020567
510k NumberK020567
Device Name:AKUPORT M1
ClassificationDevice, Galvanic Skin Response Measurement
Applicant VIBRANT HEALTH 150 DES GRANDS COTEAUX Beoeil, Quebec,  CA J3g 2c9
ContactStephen Emond
CorrespondentStephen Emond
VIBRANT HEALTH 150 DES GRANDS COTEAUX Beoeil, Quebec,  CA J3g 2c9
Product CodeGZO  
CFR Regulation Number882.1540 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received2002-02-20
Decision Date2002-05-02

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