Primary Device ID | G51015540 |
NIH Device Record Key | 015530a5-694c-485a-b9af-8e6b40d936ce |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | SIGNATURE SERIES |
Version Model Number | 1554 |
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 | G51015540 [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 | 2024-05-08 |
Device Publish Date | 2024-04-30 |
G51018270 - RAVE | 2024-05-15 |
G51022890 - REJUVENESSENCE | 2024-05-15 |
G51023740 - TAN AMERICA | 2024-05-15 |
G51027540 - RAVE | 2024-05-15 |
G51030930 - GENESIS | 2024-05-15 |
G51015410 - ERGOLINE | 2024-05-14 |
G51021990 - ERGOLINE | 2024-05-14 |
G51023770 - TAN AMERICA | 2024-05-14 |