Catalog Number

SW38DE50SST

Brand Name

Prelude® Guide Wire

Version/Model Number

10884450026134

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)

-

Over the Counter (OTC)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

K002289,K002289,K002289

Product Code

DQX

Product Code Name

WIRE, GUIDE, CATHETER

Public Device Record Key

0f4e8063-21dc-41c6-9d9d-d27f7cc2e579

Public Version Date

July 06, 2018

Public Version Number

3

DI Record Publish Date

September 24, 2016

Package DI Number

20884450026131

Quantity per Package

10

Contains DI Package

10884450026134

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-