Catalog Number

9807

Brand Name

Kendall

Version/Model Number

9807

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

Yes

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

KMF

Product Code Name

Bandage, liquid

Public Device Record Key

6fcc4728-1af5-4d34-adca-4103c042663b

Public Version Date

June 19, 2020

Public Version Number

4

DI Record Publish Date

June 30, 2018

Package DI Number

20884521024080

Quantity per Package

50

Contains DI Package

30884521024087

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

CASE