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Medison Co., Ltd.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
24
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K103397ACCUVIX XG DIAGNOSTIC ULTRASOUND SYSTEMFebruary 25, 2011
K103722THE SONOACE R5 DIAGNOSTIC ULTRASOUND SYSTEMJanuary 5, 2011
K102065SONOACE R7 DIAGNOSTIC ULTRASOUND SYSTEMAugust 6, 2010
K101455EKO 7 DIAGNOSTIC ULTRASOUND SYSTEMJuly 19, 2010
K101829THE SONOACE R3 DIAGNOSTIC ULTRASOUND SYSTEMJuly 16, 2010
K100186MYSONO U5 DIAGNOSTIC ULTRASOUND SYSTEMMarch 24, 2010
K093849ACCUVIX V10 DIAGNOSTIC ULTRASOUND SYSTEMJanuary 19, 2010
K093714SONOACE X8 DIAGNOSTIC ULTRASOUND SYSTEMDecember 10, 2009
K092159ACCUVIX V20 DIAGNOSTIC ULTRASOUND SYSTEMJuly 28, 2009
K081676SONOACE X6 DIAGNOSTIC ULTRASOUND SYSTEMJuly 2, 2008
K080800ACCUVIX V20 DIAGNOSTIC ULTRASOUND SYSTEMApril 7, 2008
K070813ACCUVIX V10 DIAGNOSTIC ULTRASOUND SYSTEMApril 10, 2007
K063580SONOACE X8 DIAGNOSTIC ULTRASOUND SYSTEMDecember 14, 2006
K061213SONOACE PICO DIAGNOSTIC ULTRASOUND SYSTEMMay 16, 2006
K060087ACCUVIX V7 DIAGNOSTIC ULTRASOUND SYSTEMJanuary 24, 2006
K053530SONOACE X4 DIAGNOSTIC ULTRASOUND SYSTEMJanuary 3, 2006
K052911ACCUVIX XQ DIAGNOSTIC ULTRASOUND SYSTEMOctober 31, 2005
K043455SA8000 SE DIAGNOSTIC ULTRASOUND SYSTEMDecember 21, 2004
K031886SONOVIEW PRO BY MEDISON CO., LTD.June 30, 2003
K002491COMBISON 301 PW ULTRASOUND SYSTEM AND TRANSDUCERSAugust 25, 2000