Catalog Number

-

Brand Name

Sense System with IBT Electrodes

Version/Model Number

70101-9-3

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)

Yes

Over the Counter (OTC)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

K182112

Product Code

GXY

Product Code Name

Electrode, Cutaneous

Public Device Record Key

a080f5a3-f545-4297-9611-6cff84ac0483

Public Version Date

March 03, 2021

Public Version Number

1

DI Record Publish Date

February 23, 2021

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-