Catalog Number

-

Brand Name

Walmart

Version/Model Number

69002WM

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"

Yes

For Single-Use

-

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

-

Product Code

FXX

Product Code Name

Mask, Surgical

Public Device Record Key

b2b67fda-896c-4971-86fd-8a07230761ba

Public Version Date

May 06, 2020

Public Version Number

3

DI Record Publish Date

January 20, 2017

Package DI Number

20681131161750

Quantity per Package

2

Contains DI Package

00681131161756

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

box