Catalog Number

-

Brand Name

Electronic Blood Pressure Monitor

Version/Model Number

PG-800A3

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)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

K131569,K131569

Product Code

DXN

Product Code Name

System, Measurement, Blood-Pressure, Non-Invasive

Public Device Record Key

5538a1f7-0d7b-412b-8e11-51663f922b57

Public Version Date

November 08, 2019

Public Version Number

4

DI Record Publish Date

November 23, 2016

Package DI Number

06948423800637

Quantity per Package

1

Contains DI Package

06948423800446

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-