The following data is part of a premarket notification filed by Neurovision Medical Product Inc. with the FDA for Neurovision Nerve Locator Monitor (nerveana), Emgview Software.
| Device ID | K170677 |
| 510k Number | K170677 |
| Device Name: | Neurovision Nerve Locator Monitor (Nerveana), EMGView Software |
| Classification | Stimulator, Electrical, Evoked Response |
| Applicant | Neurovision Medical Product Inc. 353 San Jon Rd Ventura, CA 93001 |
| Contact | Christine Vergely |
| Correspondent | Christine Vergely Neurovision Medical Product Inc. 353 San Jon Rd Ventura, CA 93001 |
| Product Code | GWF |
| CFR Regulation Number | 882.1870 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2017-03-06 |
| Decision Date | 2017-04-05 |