Catalog Number

-

Brand Name

Quick Temp Pro Infrared Thermometer

Version/Model Number

GP-300

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

MRI safety Status

MR Unsafe

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

FQZ

Product Code Name

Thermometer, Clinical Color Change

Public Device Record Key

64024a57-a22f-474d-b528-e89544167aed

Public Version Date

October 01, 2020

Public Version Number

1

DI Record Publish Date

September 23, 2020

Package DI Number

10850632007611

Quantity per Package

100

Contains DI Package

00850632007614

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Outer Carton