E-Woo Technology is one of 20523 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
E-Woo Technology - FDA 510(k) Cleared Devices
Recent clearances: DIGITAL FLAT PANEL X-RAY DETECTOR, MODEL XMARU 1717, MEDICAL IMAGE PROCESSING UNIT, MODEL EZSENSOR, COMPUTED TOMOGRAPHY X-RAY SYSTEM, MODEL PICASSO-DUO
7
Total
7
Cleared
0
Denied
E-Woo Technology has 7 FDA 510(k) cleared medical devices. Based in Sound Beach, US.
Historical record: 7 cleared submissions from 2007 to 2010. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by E-Woo Technology Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Tuv Rheinland of North America, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - E-Woo Technology
7 devices
Cleared
Aug 09, 2010
DIGITAL FLAT PANEL X-RAY DETECTOR, MODEL XMARU 1717
Radiology
480d
Cleared
Dec 02, 2009
MEDICAL IMAGE PROCESSING UNIT, MODEL EZSENSOR
Radiology
279d
Cleared
Oct 09, 2009
COMPUTED TOMOGRAPHY X-RAY SYSTEM, MODEL PICASSO-DUO
Radiology
185d
Cleared
Apr 30, 2009
COMPUTED TOMOGRAPHY X-RAY SYSTEM, PAX-REVE3D
Radiology
97d
Cleared
Oct 31, 2008
MASTER3DS
Radiology
71d
Cleared
Aug 21, 2008
PICASSO MASTER, ECT AND MASTER 3D
Radiology
52d
Cleared
Apr 05, 2007
DENTAL DIGITAL PANORAMIC/3D IMAGING SYSTEM
Radiology
27d