Catalog Number

-

Brand Name

Vicks

Version/Model Number

VNT200US

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

FLL

Product Code Name

Thermometer, Electronic, Clinical

Public Device Record Key

8aee0b65-8a4e-492e-91f3-8996cc145c8b

Public Version Date

December 04, 2020

Public Version Number

2

DI Record Publish Date

September 29, 2020

Package DI Number

20328785002038

Quantity per Package

12

Contains DI Package

00328785002034

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

CASE