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 |