Catalog Number

48762

Brand Name

Halyard

Version/Model Number

48762

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

K220547,K220547,K220547

Product Code

LZA

Product Code Name

Polymer patient examination glove

Public Device Record Key

e72b092a-42ec-41ed-aa2c-b45678c21988

Public Version Date

June 14, 2022

Public Version Number

1

DI Record Publish Date

June 06, 2022

Package DI Number

30680651487620

Quantity per Package

10

Contains DI Package

20680651487623

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

CS