Catalog Number

USEGS14-300A

Brand Name

Guidewire

Version/Model Number

SGW-060-01

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

K021990,K021990,K021990

Product Code

DQX

Product Code Name

Wire, Guide, Catheter

Public Device Record Key

61cda3e7-fe30-4c1e-90c3-31258061b04f

Public Version Date

December 22, 2021

Public Version Number

4

DI Record Publish Date

January 24, 2017

Package DI Number

10841268100487

Quantity per Package

5

Contains DI Package

00841268100480

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Shelf Box