Catalog Number

-

Brand Name

acurio

Version/Model Number

AS-302

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

K180685,K180685

Product Code

DQA

Product Code Name

Oximeter

Public Device Record Key

880e69fb-07cf-4c2a-9a25-5ae1a1551ced

Public Version Date

June 02, 2022

Public Version Number

1

DI Record Publish Date

May 25, 2022

Package DI Number

16972382160256

Quantity per Package

100

Contains DI Package

06972382160266

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-