| Primary Device ID | 08600027360068 |
| NIH Device Record Key | 15ad6427-8d35-4afe-b3a3-2755b4bbbe9a |
| Commercial Distribution Discontinuation | 2020-02-10 |
| Commercial Distribution Status | Not in Commercial Distribution |
| Brand Name | ProAlert 570 |
| Version Model Number | ProAlert 570 |
| Catalog Number | ProAlert 570 |
| Company DUNS | 047024617 |
| Company Name | JERON ELECTRONIC SYSTEMS, INC. |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | true |
| 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 | false |
| 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 | false |
| OTC Over-The-Counter | false |