| Primary Device ID | 00884838085657 |
| NIH Device Record Key | bcf60893-9d12-4582-a2d0-eaa747bf8812 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Senior Living Alert Device AutoAlert |
| Version Model Number | 300000340591 |
| Catalog Number | FD100-SL |
| Company DUNS | 080030042 |
| Company Name | Lifeline Systems Company |
| 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 | true |
| Manufacturing Date | true |
| 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 | true |