Catalog Number

-

Brand Name

iProvèn

Version/Model Number

Oxi-27

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

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

K140582

Product Code

DQA

Product Code Name

Oximeter

Public Device Record Key

6356fc0f-0e4f-4ee0-8226-b9f8397fcfc3

Public Version Date

November 10, 2021

Public Version Number

3

DI Record Publish Date

March 16, 2018

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-