Catalog Number

-

Brand Name

Light Module

Version/Model Number

NL-SK-3

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

MRI safety Status

Labeling does not contain MRI Safety Information

Device required to be labeled as containing natural rubber latex or dry natural rubber (21 CFR 801.437)

-

Device labeled as "Not made with natural rubber latex"

-

For Single-Use

-

Prescription Use (Rx)

Yes

Over the Counter (OTC)

-

Kit

-

Combination Product

-

Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)

-

FDA Premarket Submission

K170585,K170585

Product Code

LBI

Product Code Name

Unit, Neonatal Phototherapy

Public Device Record Key

7242adb1-bb25-488b-af84-9f2dbb062c7c

Public Version Date

August 24, 2020

Public Version Number

3

DI Record Publish Date

November 09, 2018

Package DI Number

30852788008058

Quantity per Package

2

Contains DI Package

10852788008054

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-