Catalog Number

-

Brand Name

Q2 5ft/1.5m IV Ext Set

Version/Model Number

95727

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

K162804,K800825,K162804,K800825

Product Code

FPK

Product Code Name

Tubing, Fluid Delivery

Public Device Record Key

1f863243-9912-4db9-9a63-fd8fd04695eb

Public Version Date

July 06, 2018

Public Version Number

3

DI Record Publish Date

January 03, 2018

Package DI Number

20634624957279

Quantity per Package

50

Contains DI Package

00634624957275

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-