Catalog Number

-

Brand Name

Intersept®

Version/Model Number

CB2F57R

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

October 24, 2018

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

Yes

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

-

FDA Premarket Submission

K891687,K891687

Product Code

DTZ

Product Code Name

OXYGENATOR, CARDIOPULMONARY BYPASS

Public Device Record Key

ba00d9f3-ee94-4702-99f9-5a9fe0e325a6

Public Version Date

December 11, 2018

Public Version Number

4

DI Record Publish Date

June 12, 2015

Package DI Number

20721902401392

Quantity per Package

5

Contains DI Package

00721902401398

Package Discontinue Date

October 24, 2018

Package Status

Not in Commercial Distribution

Package Type

PK