Catalog Number

-

Brand Name

Vented Vial Adapter 20mm

Version/Model Number

8073039

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)

Yes

Over the Counter (OTC)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

K062482,K062482,K062482

Product Code

LHI

Product Code Name

Set, I.V. Fluid Transfer

Public Device Record Key

0ae799da-0903-40dd-b59e-783372ab9f57

Public Version Date

August 09, 2019

Public Version Number

5

DI Record Publish Date

April 08, 2018

Package DI Number

27290108241123

Quantity per Package

4

Contains DI Package

17290108241126

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-