Electrical Geodesics, Inc. is one of 5134 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Electrical Geodesics, Inc. - FDA 510(k) Cleared Devices
3
Total
3
Cleared
0
Denied
Electrical Geodesics, Inc. has 3 FDA 510(k) cleared medical devices. Based in Eugene, US.
Historical record: 3 cleared submissions from 2010 to 2014. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Electrical Geodesics, Inc. Filter by specialty or product code using the sidebar.
Electrical Geodesics, Inc. — FDA 510(k) Products and Clearance History
3 devices
Cleared
Feb 12, 2014
GEODESICEEG SYSTEM 400 SERIES (GES 400)
Neurology
232d
Cleared
Feb 17, 2012
GEODESIC EEG MOBILE 100 (GEM 100)
Neurology
185d
Cleared
Dec 21, 2010
GEOSOURCE
Neurology
462d