Catalog Number

-

Brand Name

Dynatron® ion™ Medium

Version/Model Number

ION-M

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

K060814,K060814

Product Code

EGJ

Product Code Name

Device, Iontophoresis, Other Uses

Public Device Record Key

9fff407a-e646-44cc-912e-4551f7678670

Public Version Date

July 06, 2018

Public Version Number

3

DI Record Publish Date

November 20, 2015

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-