Catalog Number

-

Brand Name

LPOW

Version/Model Number

HTD8813C

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

September 03, 2020

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

9636cb6b-15e4-4a6b-8c99-6fa8aff9adc6

Public Version Date

April 28, 2021

Public Version Number

3

DI Record Publish Date

September 03, 2020

Package DI Number

16970289035066

Quantity per Package

40

Contains DI Package

06970289035069

Package Discontinue Date

September 03, 2020

Package Status

Not in Commercial Distribution

Package Type

-