Catalog Number

375545

Brand Name

Selectra

Version/Model Number

IC-50-65

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

August 27, 2021

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

-

Product Code

DQY

Product Code Name

CATHETER, PERCUTANEOUS

Public Device Record Key

6a1cc842-35ec-4f0f-b83d-86873fd2f926

Public Version Date

December 22, 2021

Public Version Number

8

DI Record Publish Date

August 27, 2014

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-