Sonoscape Company Limited is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Sonoscape Company Limited - FDA 510(k) Cleared Devices
Recent clearances: S30/S40 Digital Color Doppler Ultraound System, S8 Exp/S9 Pro Portable Digital Color Doppler Ultrasound System, S22 Digital Color Doppler Ultrasound System
22
Total
22
Cleared
0
Denied
Sonoscape Company Limited has 22 FDA 510(k) cleared radiology devices. Based in Dublin, US.
Historical record: 22 cleared submissions from 2004 to 2015.
Browse the complete list of FDA 510(k) cleared radiology devices from this manufacturer. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Underwriters Laboratories, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Sonoscape Company Limited
22 devices
Cleared
Apr 28, 2015
S30/S40 Digital Color Doppler Ultraound System
Radiology
106d
Cleared
Jan 29, 2015
S8 Exp/S9 Pro Portable Digital Color Doppler Ultrasound System
Radiology
129d
Cleared
Jan 28, 2015
S22 Digital Color Doppler Ultrasound System
Radiology
121d
Cleared
Jan 05, 2015
S9 Portable Digital Color Doppler Ultrasound System
Radiology
105d
Cleared
Dec 19, 2014
S12 Digital Color Doppler Ultrasound System
Radiology
107d
Cleared
Nov 14, 2013
DIGITAL ELECTROCARDIOGRAPHS
Cardiovascular
195d
Cleared
Nov 14, 2013
DIGITAL COLOR DOPPLER ULTASOUND SYSTEM
Radiology
94d
Cleared
Oct 04, 2013
S8 EXP PORTABLE DIGITAL COLOR DOPPLER ULTRASOUND SYSTEM
Radiology
30d
Cleared
Jun 21, 2013
DIGITAL COLOR DOPPLER ULTRASOUND SYSTEM
Radiology
53d
Cleared
Jun 14, 2013
DIGITAL COLOR DOPPLER ULTRASOUND SYSTEM
Radiology
84d
Cleared
May 24, 2013
PORTABLE DIGITAL COLOR DOPPLER ULTRASOUND SYSTEM
Radiology
36d
Cleared
Apr 12, 2013
PORTABLE DIGITAL COLOR DOPPLER ULTRASOUND SYSTEM
Radiology
86d