Catalog Number

60-403

Brand Name

Post-Stop™ Epistaxis Procedure Pack

Version/Model Number

60-403

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In HIBCC

MRI safety Status

MR Safe

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)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

K972078,K972078

Product Code

EMX

Product Code Name

Balloon, Epistaxis

Public Device Record Key

3b8e93b0-d993-4c53-aab5-daf79df1e0ea

Public Version Date

August 30, 2022

Public Version Number

7

DI Record Publish Date

September 20, 2015

Package DI Number

EBES604031

Quantity per Package

1

Contains DI Package

EBES604030

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Carton