Catalog Number

-

Brand Name

Oak Ridge Products

Version/Model Number

0319-150F

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

K161180,K161180

Product Code

MMK

Product Code Name

Container, Sharps

Public Device Record Key

d12fc52f-1a54-427f-909f-91e4e555aa6d

Public Version Date

March 08, 2021

Public Version Number

3

DI Record Publish Date

September 22, 2016

Package DI Number

10852482006516

Quantity per Package

24

Contains DI Package

00852482006519

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Case