Catalog Number

-

Brand Name

ICU Medical

Version/Model Number

B9900-446

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

K964435,K964435

Product Code

FMG

Product Code Name

Stopcock, i.V. Set

Public Device Record Key

95287c1e-5ba3-4310-a8cc-1e7fcead1653

Public Version Date

April 07, 2021

Public Version Number

7

DI Record Publish Date

July 10, 2017

Package DI Number

10840619046269

Quantity per Package

25

Contains DI Package

00840619046262

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-