Catalog Number

-

Brand Name

WristOx2 ® Pulse Oximeter

Version/Model Number

3150WB-SU

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

MRI safety Status

MR Unsafe

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)

Yes

Over the Counter (OTC)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

K102350,K102350

Product Code

DQA

Product Code Name

Oximeter

Public Device Record Key

6be4dd5d-af4a-424f-9cfb-ff5f21f51ba0

Public Version Date

November 10, 2021

Public Version Number

2

DI Record Publish Date

November 24, 2020

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-