Catalog Number

425-135-01

Brand Name

Turbo Elite™

Version/Model Number

425-135-01

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

February 06, 2019

Issuing Agency

In HIBCC

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

MCW

Product Code Name

Catheter, Peripheral, Atherectomy

Public Device Record Key

a5bad744-7b42-4b8e-a780-aa39b437b401

Public Version Date

October 26, 2021

Public Version Number

4

DI Record Publish Date

August 28, 2014

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-