Catalog Number

-

Brand Name

SANITY

Version/Model Number

JPD-FR300

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

K172795

Product Code

FLL

Product Code Name

Thermometer, Electronic, Clinical

Public Device Record Key

a111403e-a46a-4ab2-b302-4a6fde5b7df9

Public Version Date

May 23, 2022

Public Version Number

2

DI Record Publish Date

September 29, 2021

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-