Catalog Number

-

Brand Name

Suhui

Version/Model Number

Nitrile

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)

Yes

Over the Counter (OTC)

Yes

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

K211778

Product Code

LZA

Product Code Name

Polymer Patient Examination Glove

Public Device Record Key

0e69ead5-4849-4a26-a9d5-8b5b1ecc60a0

Public Version Date

October 29, 2021

Public Version Number

1

DI Record Publish Date

October 21, 2021

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-