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FDA 510(k) Applications Submitted by SUZUKEN CO., LTD.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K001896
06/21/2000
KENZ ECG 108 SINGLE CHANNEL DIGITAL ELECTROCARDIOGRAPHS; KENZ ECG 110 SINGLE CHANNEL DIGITAL ELECTROCARDIOGRAPHS WITH EC
SUZUKEN CO., LTD.
K092389
08/05/2009
DISPOSAL ECG ELECTRODES, MODEL EASYRODE
SUZUKEN CO., LTD.
K101024
04/13/2010
KENZ CARDY302 MAX
SUZUKEN CO., LTD.
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