Catalog Number

EVIVA_NG09L

Brand Name

Eviva Needle Guide

Version/Model Number

EVIVA_NG09L

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

K042290

Product Code

KNW

Product Code Name

INSTRUMENT, BIOPSY

Public Device Record Key

84479fcb-b1ec-4b42-a917-26cfc062e27c

Public Version Date

July 12, 2019

Public Version Number

4

DI Record Publish Date

August 11, 2016

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-