LOGIQ 3

System, Imaging, Pulsed Doppler, Ultrasonic

GENERAL ELECTRIC CO.

The following data is part of a premarket notification filed by General Electric Co. with the FDA for Logiq 3.

Pre-market Notification Details

Device IDK020263
510k NumberK020263
Device Name:LOGIQ 3
ClassificationSystem, Imaging, Pulsed Doppler, Ultrasonic
Applicant GENERAL ELECTRIC CO. P.O. BOX 414 Milwaukee,  WI  53201
ContactAllen Schuh
CorrespondentAllen Schuh
GENERAL ELECTRIC CO. P.O. BOX 414 Milwaukee,  WI  53201
Product CodeIYN  
CFR Regulation Number892.1550 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeSpecial
3rd Party ReviewedNo
Combination ProductNo
Date Received2002-01-25
Decision Date2002-02-06
Summary:summary

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