Neurosoft, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Neurosoft, Inc. - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
Neurosoft, Inc. has 4 FDA 510(k) cleared medical devices. Based in El Paso, US.
Historical record: 4 cleared submissions from 2000 to 2001. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Neurosoft, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Neurosoft, Inc.
4 devices
Cleared
Sep 19, 2001
NEUROSOFT'S SOURCE
Neurology
149d
Cleared
Feb 05, 2001
CURRY MULTIMODAL NEUROIMAGING SOFTWARE
Neurology
237d
Cleared
Nov 24, 2000
NEURO SCAN MEDICAL STSTEMS, MODEL MEDICOR 8
Neurology
175d
Cleared
May 17, 2000
NEURO SCAN MEDICAL SYSTEMS, MODELS 302L MEDICOR (LABORATORY) AND 302P...
Neurology
65d