Catalog Number

-

Brand Name

NA

Version/Model Number

1231-050M

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

K070431,K070431

Product Code

FYA

Product Code Name

Gown, Surgical

Public Device Record Key

046f6a8a-8ccb-4d57-99ae-bc69e3c1f00a

Public Version Date

April 07, 2021

Public Version Number

5

DI Record Publish Date

November 30, 2016

Package DI Number

10849296005255

Quantity per Package

24

Contains DI Package

00849296005258

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-