Catalog Number

-

Brand Name

Set, I.V. Fluid Transfer

Version/Model Number

17789HP

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"

Yes

For Single-Use

Yes

Prescription Use (Rx)

-

Over the Counter (OTC)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

K850757,K850757

Product Code

LHI

Product Code Name

Set, I.V. Fluid Transfer

Public Device Record Key

5051fc04-2a39-4117-85a9-db663a2528e4

Public Version Date

February 19, 2021

Public Version Number

5

DI Record Publish Date

May 26, 2016

Package DI Number

10816513020056

Quantity per Package

50

Contains DI Package

00816513020059

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

BOX