| Primary Device ID | G5100734 |
| NIH Device Record Key | d22bb9aa-c395-4802-a557-cb2990a5d58c |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | NEVADA SUN |
| Version Model Number | 0734 |
| 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 | G5100734 [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 | 2024-10-07 |
| Device Publish Date | 2024-09-27 |
| G5100734 | 0734 |
| G51007330 | 0733 |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() NEVADA SUN 77150330 3443847 Dead/Cancelled |
Light Sources, Inc. 2007-04-06 |