Catalog Number

989803151951

Brand Name

NA

Version/Model Number

989803151951

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)

Yes

Device labeled as "Not made with natural rubber latex"

-

For Single-Use

Yes

Prescription Use (Rx)

-

Over the Counter (OTC)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

-

Product Code

KLK

Product Code Name

Monitor, oxygen, cutaneous, for infant not under gas anesthesia

Public Device Record Key

23877ff7-3c33-423f-8c95-8c4e01e85471

Public Version Date

December 07, 2020

Public Version Number

4

DI Record Publish Date

February 14, 2017

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-