| Primary Device ID | 00850052003739 |
| NIH Device Record Key | 315f621c-c089-4b54-9b0d-97ab9215ab5c |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | LeukoStrat |
| Version Model Number | 850052003739 |
| Catalog Number | K4120361 |
| Company DUNS | 836976779 |
| Company Name | INVIVOSCRIBE, INC. |
| Device Count | 1 |
| DM Exempt | true |
| Pre-market Exempt | false |
| MRI Safety Status | Labeling does not contain MRI Safety Information |
| Human Cell/Tissue Product | false |
| Device Kit | true |
| Device Combination Product | false |
| Single Use | false |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | false |
| Expiration Date | true |
| 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 | 00850052003739 [Primary] |
| OWD | Somatic Gene Mutation Detection System |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 2 |
| Public Version Date | 2021-01-19 |
| Device Publish Date | 2020-06-08 |
| 00850052003685 | The LeukoStrat CDx FLT3 Mutation Assay targets regions of the FLT3 gene to identify internal tan |
| 00850052003739 | The LeukoStrat CDx FLT3 Mutation Assay is a PCR-based in vitro diagnostic test designed to detec |
| 00810022732571 | The LeukoStrat CDx FLT3 Mutation Assay is a PCR-based in vitro diagnostic test designed to detec |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() LEUKOSTRAT 86560545 5628108 Live/Registered |
INVIVOSCRIBE, INC. 2015-03-11 |
![]() LEUKOSTRAT 76693161 not registered Dead/Abandoned |
InVivoScribe Technologies LLC 2008-09-29 |