| Primary Device ID | G51018170 |
| NIH Device Record Key | 6ffc9a7c-d333-48dc-9c79-9a5b33136c1f |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | SIGNATURE SERIES |
| Version Model Number | 1817 |
| Company DUNS | 075058495 |
| Company Name | Light Sources, 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 | true |
| Serial Number | false |
| Manufacturing Date | true |
| Expiration Date | true |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | true |
| RX Perscription | false |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| HIBCC | G51018170 [Primary] |
| LEJ | Booth, Sun Tan |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2025-02-12 |
| Device Publish Date | 2025-02-04 |
| G51015540 | 1554 |
| G51030550 | 3055 |
| G51030490 | 3049 |
| G51029100 | 2910 |
| G51029120 | 2912 |
| G51029130 | 2913 |
| G51029080 | 2908 |
| G5101390 | 1390 |
| G5101568 | FR2000/VHO/BP/2.4/210 |
| G51019010 | 1901 |
| G51018610 | 1861 |
| G51018170 | 1817 |
| G51018130 | 1813 |
| G51011560 | 1156 |
| G51011480 | 1148 |
| G51015890 | 1589 |
| G51015820 | 1582 |
| G51029110 | 2911 |
| G5101412 | 1412 |