Catalog Number

KN-2719RBT500P

Brand Name

K-Pack II Needle

Version/Model Number

KN-2719RBT500P

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

K132233,K132233,K132233

Product Code

FMI

Product Code Name

Needle, Hypodermic, Single Lumen

Public Device Record Key

dfaf5564-5119-4f7d-b845-452c92c30753

Public Version Date

December 23, 2020

Public Version Number

1

DI Record Publish Date

December 15, 2020

Package DI Number

35413206250173

Quantity per Package

500

Contains DI Package

05413206250172

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Shelfbox