Catalog Number

-

Brand Name

hcs

Version/Model Number

HCS3014

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

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

b1c64295-67fe-4fdc-bf05-acee4ca8a898

Public Version Date

November 30, 2021

Public Version Number

3

DI Record Publish Date

December 31, 2019

Package DI Number

10849027001259

Quantity per Package

6

Contains DI Package

00849027001252

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

case