Catalog Number

406L

Brand Name

Advocate Arm BPM L Cuff

Version/Model Number

406L

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

K150430,K150430,K150430

Product Code

DXN

Product Code Name

System, Measurement, Blood-Pressure, Non-Invasive

Public Device Record Key

30de9ef5-8eac-4baf-9cd1-1083c13a35d1

Public Version Date

November 09, 2020

Public Version Number

7

DI Record Publish Date

August 22, 2016

Package DI Number

10894046001414

Quantity per Package

3

Contains DI Package

00894046001417

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

406L-I