Primary Device ID | G51026300 |
NIH Device Record Key | 1cf1ccdb-a27a-4d37-9c31-27b9cd04199b |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | CABANA SOL |
Version Model Number | 2630 |
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 | G51026300 [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 | 2024-09-17 |
Device Publish Date | 2024-09-09 |
G51032510 | 3251 |
G51026350 | 2635 |
G51026310 | 2631 |
G51026300 | 2630 |
G51026290 | 2629 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
CABANA SOL 77169866 not registered Dead/Abandoned |
brosseau michel 2007-05-01 |