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Suzuken Co., Ltd.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
13
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K172068Kenz Cardico1211June 1, 2018
K101024KENZ CARDY302 MAXJanuary 6, 2011
K092389DISPOSAL ECG ELECTRODES, MODEL EASYRODEOctober 13, 2009
K001896KENZ ECG 108 SINGLE CHANNEL DIGITAL ELECTROCARDIOGRAPHS; KENZ ECG 110 SINGLE CHANNEL DIGITAL ELECTROJanuary 8, 2001
K870443KENZ-CARDICO 1201July 1, 1987
K862544KENZ-ECG-102 SINGLE CHANNEL ELECTROCARDIOGRAPHAugust 6, 1986
K843731KENZ 80Z MARK IIJuly 11, 1985
K822968ELECTROCARDIOGRAPH INTERPRETERDecember 15, 1982
K820854KENZ-45MJune 1, 1982
K820991KENZ-GELECT GEL PADApril 26, 1982
K812263KENZ-GELECTNovember 2, 1981
K811949KENL-ECG-3August 13, 1981
K811950KENL-ECGAugust 13, 1981