Catalog Number

5050-FSD

Brand Name

Medical Science Products

Version/Model Number

5050-FSD

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

GXY

Product Code Name

Electrode, Cutaneous

Public Device Record Key

cb64b2b5-26f8-4ef0-8eb5-306c380a6ba6

Public Version Date

February 19, 2021

Public Version Number

3

DI Record Publish Date

August 08, 2017

Package DI Number

10864666000395

Quantity per Package

400

Contains DI Package

00864666000398

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Box