Catalog Number

6010

Brand Name

Tech-Med

Version/Model Number

6010

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

November 06, 2018

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)

Yes

Over the Counter (OTC)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

K032720,K032720

Product Code

GZJ

Product Code Name

STIMULATOR, NERVE, TRANSCUTANEOUS, FOR PAIN RELIEF

Public Device Record Key

ea6490d6-ea0e-49c7-ae52-5e0722cfb6df

Public Version Date

May 23, 2022

Public Version Number

6

DI Record Publish Date

September 24, 2016

Package DI Number

20665973016782

Quantity per Package

30

Contains DI Package

00665973016788

Package Discontinue Date

November 06, 2018

Package Status

Not in Commercial Distribution

Package Type

Case