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 |