Catalog Number

-

Brand Name

Dr. Talbot's

Version/Model Number

14922

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)

Yes

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

-

Product Code

OCH

Product Code Name

Oximeter, Infrared, Sporting, Aviation

Public Device Record Key

b1d00057-819f-44d3-b6c5-5b8c13dcb9ba

Public Version Date

November 10, 2021

Public Version Number

2

DI Record Publish Date

October 23, 2020

Package DI Number

20370797149225

Quantity per Package

6

Contains DI Package

00370797149221

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-