Catalog Number

-

Brand Name

AEON

Version/Model Number

A310L

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)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

K190869,K190869

Product Code

DQA

Product Code Name

Oximeter

Public Device Record Key

86ebb829-fde6-444e-ac2a-62fc7ca5c57e

Public Version Date

November 10, 2021

Public Version Number

2

DI Record Publish Date

September 18, 2019

Package DI Number

36947832500108

Quantity per Package

100

Contains DI Package

06947832500084

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-