Catalog Number

-

Brand Name

ViSi

Version/Model Number

NIBP Adapter

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)

Yes

Over the Counter (OTC)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

K152341,K152341

Product Code

DXN

Product Code Name

System, Measurement, Blood-Pressure, Non-Invasive

Public Device Record Key

c11a71cc-1454-4d19-8c07-4ce3c25449cf

Public Version Date

May 16, 2022

Public Version Number

8

DI Record Publish Date

September 19, 2016

Package DI Number

10850733007039

Quantity per Package

15

Contains DI Package

00850733007032

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Case