Catalog Number

518-062

Brand Name

LLD EZ™

Version/Model Number

518-062

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

February 06, 2019

Issuing Agency

In HIBCC

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)

Yes

Over the Counter (OTC)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

K142116,K142116

Product Code

DRB

Product Code Name

Stylet, Catheter

Public Device Record Key

c19acf67-a9af-40f3-b22a-386b5039abba

Public Version Date

October 26, 2021

Public Version Number

5

DI Record Publish Date

August 19, 2014

Package DI Number

M2045180621

Quantity per Package

3

Contains DI Package

M2045180620

Package Discontinue Date

February 06, 2019

Package Status

Not in Commercial Distribution

Package Type

Box