Catalog Number

-

Brand Name

Deltec

Version/Model Number

21-3369-24

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)

Yes

Over the Counter (OTC)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

K072657,K072657

Product Code

FPA

Product Code Name

Set, administration, intravascular

Public Device Record Key

80ccf93e-e8ab-46a7-a5b6-a8a9eafb814d

Public Version Date

August 17, 2018

Public Version Number

4

DI Record Publish Date

October 13, 2016

Package DI Number

30610586033029

Quantity per Package

12

Contains DI Package

10610586033025

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

BOX