Catalog Number

V10-0014

Brand Name

Patient Stop Cable (Model TS4 and Lumenair™)

Version/Model Number

Model Lumenair

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

K033617

Product Code

DRN

Product Code Name

Device, counter-pulsating, external

Public Device Record Key

6dd2ef68-4ca8-48f7-bd73-72b4333b57bd

Public Version Date

July 06, 2018

Public Version Number

3

DI Record Publish Date

November 29, 2016

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-