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.


Search | Companies | Product Codes | Device Names | Contacts | Applications | Decisions | Contact