Catalog Number

FP_400202

Brand Name

Finapres

Version/Model Number

Finger cuff size Small

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

K023338,K023723,K063111,K141460,K160967

Product Code

DSB

Product Code Name

Plethysmograph, Impedance

Public Device Record Key

9cf6e335-b17a-415d-b2bb-6d3a71bf58dc

Public Version Date

December 03, 2018

Public Version Number

5

DI Record Publish Date

September 24, 2016

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-