Catalog Number

-

Brand Name

iChoice

Version/Model Number

OX200

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)

-

Over the Counter (OTC)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

-

Product Code

PGJ

Product Code Name

Oximeter, Wellness

Public Device Record Key

40884546-5013-4a59-a852-1b6c9e0816d2

Public Version Date

November 10, 2021

Public Version Number

3

DI Record Publish Date

March 20, 2019

Package DI Number

10846841019378

Quantity per Package

48

Contains DI Package

00846841019371

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-