Catalog Number

-

Brand Name

LUMISCOPE

Version/Model Number

1133

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In HIBCC

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

-

Product Code

DXN

Product Code Name

System, Measurement, Blood-Pressure, Non-Invasive

Public Device Record Key

6d7abaa1-6e7f-4696-8ec4-c464ebc7fa28

Public Version Date

August 27, 2020

Public Version Number

5

DI Record Publish Date

August 31, 2016

Package DI Number

M36811333

Quantity per Package

4

Contains DI Package

M36811332

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-