| Primary Device ID | G51019600 |
| NIH Device Record Key | 628959a9-634a-4d6d-a006-57f19c3532ee |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | SUN MASTER |
| Version Model Number | 1960 |
| 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 | G51019600 [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 | 2024-06-12 |
| Device Publish Date | 2024-06-04 |
| G51021560 | SUNMASTER CLEARTECH 20 F71/HO/BP/ SOL65 GR |
| G51024860 | 2486 |
| G51024850 | 2485 |
| G51021370 | 2137 |
| G51021350 | 2135 |
| G51019600 | 1960 |
| G51019590 | 1959 |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() SUN MASTER 85077223 3959827 Live/Registered |
Lumite, Inc. 2010-07-02 |
![]() SUN MASTER 76598586 not registered Dead/Abandoned |
THE AWNING WAREHOUSE, INC. 2004-06-21 |
![]() SUN MASTER 74258279 1772369 Live/Registered |
SUMMIT HILL, INC. 1992-03-23 |
![]() SUN MASTER 73625519 1469066 Dead/Cancelled |
HOME & ROAM LEISURE, INC. 1986-10-16 |
![]() SUN MASTER 73366775 1260933 Live/Registered |
California Umbrella Sales, Inc. 1982-05-27 |
![]() SUN MASTER 73254776 1164668 Dead/Cancelled |
Louverdrape, Inc. 1980-03-20 |