Neuro Resource Group, Inc. is one of 5196 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Neuro Resource Group, Inc. - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
Neuro Resource Group, Inc. has 4 FDA 510(k) cleared medical devices. Based in Irving, US.
Historical record: 4 cleared submissions from 2005 to 2013. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Neuro Resource Group, Inc. Filter by specialty or product code using the sidebar.
Neuro Resource Group, Inc. — FDA 510(k) Products and Clearance History
4 devices
Cleared
Jun 21, 2013
INTERX STERILE SELF-ADHESIVE DUAL ELECTRODE (ISSDE)
Neurology
88d
Cleared
Apr 04, 2008
INTERX 1000/DERMA 200 STIMULATOR FOR COSMETIC USE
Neurology
437d
Cleared
Mar 29, 2006
INTERX500 FLEXIBLE ARRAY ELECTRODE
Neurology
91d
Cleared
May 17, 2005
INTERX5000
Neurology
208d