Catalog Number

590-001

Brand Name

Bridge™

Version/Model Number

590-001AB

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

K153530

Product Code

MJN

Product Code Name

Catheter, Intravascular Occluding, Temporary

Public Device Record Key

37171913-f932-4619-a22b-12c532de0c6b

Public Version Date

October 26, 2021

Public Version Number

5

DI Record Publish Date

October 19, 2017

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-