Catalog Number

3037-01

Brand Name

VitalPatch 2.0

Version/Model Number

3037-01

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

MRI safety Status

MR Unsafe

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

K190916,K190916

Product Code

DRG

Product Code Name

Transmitters And Receivers, Physiological Signal, Radiofrequency

Public Device Record Key

63d57c45-814e-4674-bf48-827a3f9db363

Public Version Date

November 11, 2020

Public Version Number

1

DI Record Publish Date

November 03, 2020

Package DI Number

00850490007245

Quantity per Package

20

Contains DI Package

00850490007238

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

bag