The following data is part of a premarket notification filed by Neurocom International, Inc. with the FDA for Equitest.
| Device ID | K851744 | 
| 510k Number | K851744 | 
| Device Name: | EQUITEST | 
| Classification | Apparatus, Vestibular Analysis | 
| Applicant | NEUROCOM INTERNATIONAL, INC. 2326 NW LOVEJOY ST. P.O. BOX 12529 Portland, OR 97210 | 
| Contact | Lewis M Nashner | 
| Correspondent | Lewis M Nashner NEUROCOM INTERNATIONAL, INC. 2326 NW LOVEJOY ST. P.O. BOX 12529 Portland, OR 97210 | 
| Product Code | LXV | 
| CFR Regulation Number | 510(k) Premarket Notification [🔎] | 
| Decision | Substantially Equivalent (SESE) | 
| Type | Traditional | 
| 3rd Party Reviewed | No | 
| Combination Product | No | 
| Date Received | 1985-04-29 | 
| Decision Date | 1985-08-05 | 
| Mark Image Registration | Serial | Company Trademark Application Date | 
|---|---|
|  EQUITEST  90261594  not registered Live/Pending | Nezikist Group LTD 2020-10-18 | 
|  EQUITEST  76418583  2785646 Live/Registered | NATUS MEDICAL INCORPORATED 2002-06-07 | 
|  EQUITEST  73623045  1446204 Live/Registered | NEUROCOM INTERNATIONAL, INC. 1986-09-26 |