Catalog Number

-

Brand Name

ProGear

Version/Model Number

FM80120

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)

-

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

5d9b17cd-e538-42cd-8c71-5d43af873cc9

Public Version Date

May 06, 2020

Public Version Number

3

DI Record Publish Date

September 26, 2016

Package DI Number

20852212003072

Quantity per Package

6

Contains DI Package

00852212003078

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Case