Catalog Number

112-691-000

Brand Name

Kroger

Version/Model Number

112-691-000

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

FLL

Product Code Name

Thermometer, Electronic, Clinical

Public Device Record Key

08052b8e-e632-49a2-b2ae-bc5346a336e0

Public Version Date

March 29, 2018

Public Version Number

2

DI Record Publish Date

July 18, 2016

Package DI Number

10011110793802

Quantity per Package

12

Contains DI Package

30011110793806

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Master Carton