Catalog Number

-

Brand Name

Vicks

Version/Model Number

V925P-A-V

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

K051100,K051100

Product Code

FLL

Product Code Name

Thermometer, Electronic, Clinical

Public Device Record Key

007a29f1-5090-4b60-b8bc-cbddc9c71294

Public Version Date

May 27, 2020

Public Version Number

4

DI Record Publish Date

September 09, 2016

Package DI Number

10328785000433

Quantity per Package

12

Contains DI Package

00328785000436

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Case