Medison Co., Ltd. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Medison Co., Ltd. - FDA 510(k) Cleared Devices
Recent clearances: ACCUVIX XG DIAGNOSTIC ULTRASOUND SYSTEM, THE SONOACE R5 DIAGNOSTIC ULTRASOUND SYSTEM, SONOACE R7 DIAGNOSTIC ULTRASOUND SYSTEM
24
Total
24
Cleared
0
Denied
Medison Co., Ltd. has 24 FDA 510(k) cleared radiology devices. Based in Media, US.
Historical record: 24 cleared submissions from 1990 to 2011.
Browse the complete list of FDA 510(k) cleared radiology devices from this manufacturer. Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Regulatory Technology Services, LLC, Entela, Inc. and Tuv Product Service, Inc..
FDA 510(k) Regulatory Record - Medison Co., Ltd.
24 devices
Cleared
Feb 25, 2011
ACCUVIX XG DIAGNOSTIC ULTRASOUND SYSTEM
Radiology
98d
Cleared
Jan 05, 2011
THE SONOACE R5 DIAGNOSTIC ULTRASOUND SYSTEM
Radiology
15d
Cleared
Aug 06, 2010
SONOACE R7 DIAGNOSTIC ULTRASOUND SYSTEM
Radiology
14d
Cleared
Jul 19, 2010
EKO 7 DIAGNOSTIC ULTRASOUND SYSTEM
Radiology
55d
Cleared
Jul 16, 2010
THE SONOACE R3 DIAGNOSTIC ULTRASOUND SYSTEM
Radiology
15d
Cleared
Mar 24, 2010
MYSONO U5 DIAGNOSTIC ULTRASOUND SYSTEM
Radiology
61d
Cleared
Jan 19, 2010
ACCUVIX V10 DIAGNOSTIC ULTRASOUND SYSTEM
Radiology
34d
Cleared
Dec 10, 2009
SONOACE X8 DIAGNOSTIC ULTRASOUND SYSTEM
Radiology
8d
Cleared
Jul 28, 2009
ACCUVIX V20 DIAGNOSTIC ULTRASOUND SYSTEM
Radiology
12d
Cleared
Jul 02, 2008
SONOACE X6 DIAGNOSTIC ULTRASOUND SYSTEM
Radiology
15d
Cleared
Apr 07, 2008
ACCUVIX V20 DIAGNOSTIC ULTRASOUND SYSTEM
Radiology
17d
Cleared
Apr 10, 2007
ACCUVIX V10 DIAGNOSTIC ULTRASOUND SYSTEM
Radiology
15d