Catalog Number

-

Brand Name

Dr. Talbot's

Version/Model Number

14900

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

de7bc99e-7432-4b49-ad75-368cdd56ddef

Public Version Date

June 26, 2020

Public Version Number

1

DI Record Publish Date

June 18, 2020

Package DI Number

20370797149003

Quantity per Package

6

Contains DI Package

00370797149009

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-