Catalog Number

-

Brand Name

Vial Adapter

Version/Model Number

8072024

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

K001293,K001293,K001293

Product Code

LHI

Product Code Name

Set, I.V. Fluid Transfer

Public Device Record Key

a7b284b0-f149-4e1c-9485-533420612962

Public Version Date

July 23, 2020

Public Version Number

7

DI Record Publish Date

May 01, 2016

Package DI Number

27290108240522

Quantity per Package

4

Contains DI Package

17290108240525

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-