Catalog Number

JP-2290

Brand Name

JACKSON-PRATT

Version/Model Number

JP-2290

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

-

Product Code

KGZ

Product Code Name

ACCESSORIES, CATHETER

Public Device Record Key

66f1d192-b7c5-49af-8aa8-ea0aae06f467

Public Version Date

March 08, 2022

Public Version Number

2

DI Record Publish Date

December 09, 2021

Package DI Number

50885380182677

Quantity per Package

8

Contains DI Package

20885380182676

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

CASE