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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