Catalog Number

N589A001

Brand Name

Halyard

Version/Model Number

46731

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)

-

Over the Counter (OTC)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

K941562,K941562

Product Code

FMF

Product Code Name

Syringe, piston

Public Device Record Key

5b77c193-d551-4075-8559-a157694495f3

Public Version Date

November 16, 2018

Public Version Number

4

DI Record Publish Date

December 21, 2017

Package DI Number

30680651467318

Quantity per Package

25

Contains DI Package

10680651467314

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

CS