Wipro GE Healthcare Private, Ltd. is one of 16433 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Wipro GE Healthcare Private, Ltd. - FDA 510(k) Cleared Devices
Recent clearances: 1.5T 4CH LARGE FLEX COIL, 1.5 4CH SMALL FLEX COIL, LULLABY TM WARMER, LULLABY LED PHOTTHERAPY SYSTEM
5
Total
5
Cleared
0
Denied
Wipro GE Healthcare Private, Ltd. has 5 FDA 510(k) cleared medical devices. Based in Wwauwatosa, US.
Historical record: 5 cleared submissions from 2010 to 2013. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Wipro GE Healthcare Private, Ltd. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Wipro GE Healthcare Private, Ltd.
5 devices
Cleared
Feb 22, 2013
1.5T 4CH LARGE FLEX COIL, 1.5 4CH SMALL FLEX COIL
Radiology
84d
Cleared
Sep 14, 2012
LULLABY TM WARMER
General Hospital
105d
Cleared
May 02, 2012
LULLABY LED PHOTTHERAPY SYSTEM
General Hospital
104d
Cleared
Jul 19, 2011
MINI TELEMETRY SYSTEM
Obstetrics & Gynecology
141d
Cleared
Oct 01, 2010
GE VIVID P3 DIAGNOSTIC ULTRASOUND IMAGING SYSTEM
Radiology
66d