Catalog Number

09-332

Brand Name

Veridian

Version/Model Number

09-332

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

K051422,K051422,K051422

Product Code

FLL

Product Code Name

Thermometer, Electronic, Clinical

Public Device Record Key

cc74d617-2f39-4fda-bef6-af561df15fcf

Public Version Date

December 04, 2020

Public Version Number

4

DI Record Publish Date

September 24, 2016

Package DI Number

10845717004173

Quantity per Package

36

Contains DI Package

30845717004177

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Master