Catalog Number

-

Brand Name

ALLURA

Version/Model Number

3321-212-X

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)

Yes

Over the Counter (OTC)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

K202542

Product Code

KXP

Product Code Name

Stent, Vaginal

Public Device Record Key

9a9f18fc-578c-4964-a9fa-bb5bcea3046f

Public Version Date

November 04, 2021

Public Version Number

1

DI Record Publish Date

October 27, 2021

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-