Neurovision Medical Products, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Neurovision Medical Products, Inc. - FDA 510(k) Cleared Devices
9
Total
9
Cleared
0
Denied
Neurovision Medical Products, Inc. has 9 FDA 510(k) cleared medical devices. Based in Ventura, US.
Historical record: 9 cleared submissions from 2010 to 2013. Primary specialty: Ear, Nose, Throat.
Browse the FDA 510(k) cleared devices submitted by Neurovision Medical Products, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Neurovision Medical Products, Inc.
9 devices
Cleared
Dec 26, 2013
NEUROVISION MEDICAL MOTION SENSOR
Anesthesiology
297d
Cleared
Jul 12, 2013
NEUROVISION INK PRINTED ENDOTRACHEAL TUBE ELECTRODE
Neurology
109d
Cleared
Dec 13, 2012
SIGNAL GEAR URETHRAL CATHETER ELECTRODE
Gastroenterology & Urology
357d
Cleared
Oct 19, 2012
NONDISPOSABLE STIMULATING INSTRUMENTS
Ear, Nose, Throat
109d
Cleared
Nov 03, 2011
NEUROVISION INK PRINTED ENDOTRACHEAL TUBE ELECTRODE
Ear, Nose, Throat
209d
Cleared
Sep 30, 2011
NEUROVISION NERVE LOCATOR MONITOR
Neurology
255d
Cleared
Jun 28, 2011
DRYTOUCH SUCTION STIMULATOR PROBE
Ear, Nose, Throat
106d
Cleared
Apr 08, 2011
PAIRED HYDROGEL ELECTRODE
Ear, Nose, Throat
80d
Cleared
Dec 21, 2010
NEUROVISION SE (NERVEANA)
Ear, Nose, Throat
82d