Catalog Number

-

Brand Name

pluse oximeter

Version/Model Number

JPD-500H

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

K170965

Product Code

DQA

Product Code Name

Oximeter

Public Device Record Key

fb4953cf-884b-4bff-931b-5fe8eeb10c41

Public Version Date

November 10, 2021

Public Version Number

2

DI Record Publish Date

December 19, 2018

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-