ERGOLINE EXTREME POWER

GUDID G51021380

Light Sources, Inc.

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Primary Device ID	G51021380
NIH Device Record Key	aecff068-640a-463c-a4d2-3a42a55bf7c7
Commercial Distribution Status	In Commercial Distribution
Brand Name	ERGOLINE EXTREME POWER
Version Model Number	2138
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 Identifiers

Device Issuing Agency	Device ID
HIBCC	G51021380 [Primary]

FDA Product Code

LEJ	Booth, Sun Tan

Sterilization

Steralize Prior To Use	false
Device Is Sterile	false

Device Entry Metadata

Public Version Status	New
Device Record Status	Published
Public Version Number	1
Public Version Date	2024-05-10
Device Publish Date	2024-05-02

Devices Manufactured by Light Sources, Inc.

G51021670 - NEW TECHNOLOGY	2024-06-07
G51023610 - BE BRIGHT	2024-06-07
G51024110 - Brilliance Active Bronzer	2024-06-07
G51028250 - Brilliance Active Bronzer	2024-06-07
G51030050 - TAN PRO	2024-06-06
G51018390 - RAVE	2024-06-05
G51026590 - GENESIS	2024-06-05
G51030440 - BRILLIANCE	2024-06-05