Catalog Number

-

Brand Name

Famidoc

Version/Model Number

FDTH-V0-12

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

K072641,K072641

Product Code

FLL

Product Code Name

Thermometer, Electronic, Clinical

Public Device Record Key

0b0f2ac6-4935-4253-a075-0e52681b3b9f

Public Version Date

July 06, 2018

Public Version Number

3

DI Record Publish Date

December 29, 2016

Package DI Number

10854314007357

Quantity per Package

200

Contains DI Package

00854314007350

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-