Catalog Number

-

Brand Name

QUELL

Version/Model Number

QE-CLB

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

-

Prescription Use (Rx)

-

Over the Counter (OTC)

Yes

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

-

Product Code

NUH

Product Code Name

Stimulator, Nerve, Transcutaneous, Over-The-Counter

Public Device Record Key

f0f813cf-f512-4b7d-8003-98adf57574f2

Public Version Date

October 23, 2019

Public Version Number

3

DI Record Publish Date

March 07, 2017

Package DI Number

10851221006374

Quantity per Package

6

Contains DI Package

00851221006377

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Case