Catalog Number

BP710

Brand Name

3 Series Blood Pressure Monitor

Version/Model Number

BP710N

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

-

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

K133379,K133379,K133379

Product Code

DXN

Product Code Name

System, Measurement, Blood-Pressure, Non-Invasive

Public Device Record Key

5bed01ce-54cd-42c0-ac28-fed12bd84aa3

Public Version Date

November 08, 2019

Public Version Number

4

DI Record Publish Date

September 16, 2016

Package DI Number

10073796271043

Quantity per Package

12

Contains DI Package

00073796271046

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Case