Catalog Number

74-332

Brand Name

Meijer

Version/Model Number

74-332

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)

Yes

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

K032362,K032362,K032362

Product Code

FLL

Product Code Name

Thermometer, Electronic, Clinical

Public Device Record Key

4183afd7-2a14-4f77-a43e-2523800889c9

Public Version Date

December 04, 2020

Public Version Number

4

DI Record Publish Date

September 15, 2016

Package DI Number

10708820047737

Quantity per Package

12

Contains DI Package

30708820047731

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Master