Catalog Number

235

Brand Name

S&W

Version/Model Number

FS-VF01C

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

March 31, 2017

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"

Yes

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

-

Product Code

DRX

Product Code Name

Electrode, Electrocardiograph

Public Device Record Key

dda059f0-486a-4aa1-b5d1-525b56ded93d

Public Version Date

March 29, 2018

Public Version Number

2

DI Record Publish Date

October 24, 2015

Package DI Number

30854661006410

Quantity per Package

4

Contains DI Package

20854661006413

Package Discontinue Date

March 31, 2017

Package Status

Not in Commercial Distribution

Package Type

case