Catalog Number

-

Brand Name

ADVANCE

Version/Model Number

NC-S92

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)

Yes

Over the Counter (OTC)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

-

Product Code

JXE

Product Code Name

Device, Nerve Conduction Velocity Measurement

Public Device Record Key

02dd046e-e35f-43ed-9b06-2c95c0bb077a

Public Version Date

October 22, 2018

Public Version Number

3

DI Record Publish Date

September 08, 2016

Package DI Number

10851221006220

Quantity per Package

6

Contains DI Package

00851221006223

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Case