ULTRASOUND SCANNER 2001

System, Imaging, Pulsed Echo, Ultrasonic

B & K MEDICAL A/S

The following data is part of a premarket notification filed by B & K Medical A/s with the FDA for Ultrasound Scanner 2001.

Pre-market Notification Details

Device IDK936024
510k NumberK936024
Device Name:ULTRASOUND SCANNER 2001
ClassificationSystem, Imaging, Pulsed Echo, Ultrasonic
Applicant B & K MEDICAL A/S SANDTOFTEN 9 Dk 2820 Gentofte,  DK
ContactVilly Braender
CorrespondentVilly Braender
B & K MEDICAL A/S SANDTOFTEN 9 Dk 2820 Gentofte,  DK
Product CodeIYO  
CFR Regulation Number892.1560 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1993-12-17
Decision Date1995-08-22

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