Ultrasound Scanner System Bk2300

System, Imaging, Pulsed Doppler, Ultrasonic

BK MEDICAL APS

The following data is part of a premarket notification filed by Bk Medical Aps with the FDA for Ultrasound Scanner System Bk2300.

Pre-market Notification Details

Device IDK143298
510k NumberK143298
Device Name:Ultrasound Scanner System Bk2300
ClassificationSystem, Imaging, Pulsed Doppler, Ultrasonic
Applicant BK MEDICAL APS MILEPARKEN 34 Herlev,  DK Dk-2730
ContactRandi Hauerberg
CorrespondentRandi Hauerberg
BK MEDICAL APS MILEPARKEN 34 Herlev,  DK Dk-2730
Product CodeIYN  
Subsequent Product CodeITX
Subsequent Product CodeIYO
CFR Regulation Number892.1550 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeAbbreviated
3rd Party ReviewedNo
Combination ProductNo
Date Received2014-11-17
Decision Date2015-01-16
Summary:summary

NIH GUDID Devices

Device IdentifiersubmissionNumberSupplement
05704916000158 K143298 000

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