CLEO HPA 920669541

GUDID G6199206695411

Ultraviolet tanning device

JW NORTH AMERICA, INC.

Ultraviolet tanning device
Primary Device IDG6199206695411
NIH Device Record Keyfaa4583d-56d2-472f-9cfc-2ce954fe595c
Commercial Distribution StatusIn Commercial Distribution
Brand NameCLEO HPA
Version Model Number700 S FX
Catalog Number920669541
Company DUNS039280558
Company NameJW NORTH AMERICA, INC.
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Countertrue

Device Identifiers

Device Issuing AgencyDevice ID
HIBCCB5331181140 [Previous]
HIBCCG6199206695410 [Primary]
HIBCCG6199206695411 [Package]
Contains: G6199206695410
Package: carton box [25 Units]
In Commercial Distribution

FDA Product Code

LEJBooth, Sun Tan

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2024-08-09
Device Publish Date2024-08-01

On-Brand Devices [CLEO HPA]

G6199386702451Ultraviolet tanning device
G6199213785411Ultraviolet tanning device
G6199213761451Ultraviolet tanning device
G6199206749311Ultraviolet tanning device
G6199206695411Ultraviolet tanning device
G6199192202451Ultraviolet tanning device
G6199131388411Ultraviolet tanning device
G6199131371411Ultraviolet tanning device
G6199131340451Ultraviolet tanning device
G6199131036451Ultraviolet tanning device

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