Catalog Number

-

Brand Name

LCCS

Version/Model Number

IKD-C-30-LC

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)

Yes

Over the Counter (OTC)

-

Kit

-

Combination Product

-

Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)

-

FDA Premarket Submission

-

Product Code

IKD

Product Code Name

Cable, Electrode

Public Device Record Key

e1270708-e37a-437c-9052-d061961457ff

Public Version Date

August 02, 2021

Public Version Number

1

DI Record Publish Date

July 24, 2021

Package DI Number

14895233605626

Quantity per Package

20

Contains DI Package

04895233605629

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Box