Catalog Number

-

Brand Name

Patterson

Version/Model Number

30963

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)

Yes

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

K141759,K141759

Product Code

MMK

Product Code Name

Container, Sharps

Public Device Record Key

e90da970-371b-4765-aea9-046d6b805db8

Public Version Date

March 08, 2021

Public Version Number

3

DI Record Publish Date

July 01, 2017

Package DI Number

10889215309637

Quantity per Package

10

Contains DI Package

00889215309630

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

case