FDA 510(k) Applications Submitted by CHRISTINE VERGELY

FDA 510(k) Number Submission Date Device Name Applicant
K110138 01/18/2011 PAIRED HYDROGEL ELECTRODE NEUROVISION MEDICAL PRODUCTS, INC.
K110140 01/18/2011 NEUROVISION NERVE LOCATOR MONITOR NEUROVISION MEDICAL PRODUCTS, INC.
K130570 03/04/2013 NEUROVISION MEDICAL MOTION SENSOR NEUROVISION MEDICAL PRODUCTS, INC.
K170677 03/06/2017 Neurovision Nerve Locator Monitor (Nerveana), EMGView Software Neurovision Medical Product Inc.
K110712 03/14/2011 DRYTOUCH SUCTION STIMULATOR PROBE NEUROVISION MEDICAL PRODUCTS, INC.
K130806 03/25/2013 NEUROVISION INK PRINTED ENDOTRACHEAL TUBE ELECTRODE NEUROVISION MEDICAL PRODUCTS, INC.
K110989 04/08/2011 NEUROVISION INK PRINTED ENDOTRACHEAL TUBE ELECTRODE NEUROVISION MEDICAL PRODUCTS, INC.
K121931 07/02/2012 NONDISPOSABLE STIMULATING INSTRUMENTS NEUROVISION MEDICAL PRODUCTS, INC.
K102862 09/30/2010 NEUROVISION SE (NERVEANA) NEUROVISION MEDICAL PRODUCTS, INC.
K113771 12/22/2011 SIGNAL GEAR URETHRAL CATHETER ELECTRODE NEUROVISION MEDICAL PRODUCTS, INC.


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