Primary Device ID | 00863725000300 |
NIH Device Record Key | 4b719d29-1b5d-43da-9007-6cf4de05f149 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | NeuroQuant |
Version Model Number | NQ |
Company DUNS | 086086498 |
Company Name | CORTECHS LABS INC |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | false |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00863725000300 [Primary] |
LLZ | System, Image Processing, Radiological |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2020-02-05 |
Device Publish Date | 2016-09-24 |
00860000004824 - NeuroQuant Brain Tumor | 2024-08-07 |
00863725000300 - NeuroQuant | 2020-02-05 |
00863725000300 - NeuroQuant | 2020-02-05 |
00863725000317 - LesionQuant | 2020-02-05 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() NEUROQUANT 77067450 3528099 Live/Registered |
CorTechs Labs, Inc 2006-12-19 |