Catalog Number

-

Brand Name

N/A

Version/Model Number

DT6070

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

K110707,K110707

Product Code

NUH

Product Code Name

Stimulator, Nerve, Transcutaneous, Over-The-Counter

Public Device Record Key

fd685748-8050-4baf-bc4f-162854dd56f3

Public Version Date

February 19, 2021

Public Version Number

7

DI Record Publish Date

October 12, 2016

Package DI Number

80092237605451

Quantity per Package

30

Contains DI Package

00092237605455

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

CA