| Primary Device ID | G51031030 |
| NIH Device Record Key | 5807fe28-dd64-4ee9-ae46-a0464c9c16fb |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | KBL |
| Version Model Number | 3103 |
| 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 | G51031030 [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 | 2024-05-28 |
| Device Publish Date | 2024-05-20 |
| G51007040 - LIGHT SOURCES INC | 2024-08-12 F72T12/BL/HO/RDC/5.0B |
| G51019900 - HEARTLAND | 2024-08-12 FR71/VHO/BP/2.6/230 |
| G51019920 - HEARTLAND | 2024-08-12 FR71/VHO/BP/2.6B/180 |
| G5102961 - LIGHT SOURCES INC | 2024-08-12 FR2000/VHO/BP/8.5/230 |
| G51032140 - PROSUN | 2024-08-09 FR2000T12/BL/VHO/BP/EBX/210 |
| G51016960 - FUTURE INDUSTRIES | 2024-08-08 FR59T12/BL/HO/BP/2.6/230 |
| G51022470 - ULTRAVIOLET SOURCES INC | 2024-08-08 FR2000/VHO/BP/2.4/210 |
| G51018760 - RAVE | 2024-08-02 |