Catalog Number

07A0331

Brand Name

ABBOTT PRISM

Version/Model Number

7A03-31

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

-

Product Code

MZA

Product Code Name

TEST,EQUIPMENT,AUTOMATED BLOODBORNE PATHOGEN

Public Device Record Key

462f3815-b329-4d89-a71c-8c31089b56d3

Public Version Date

March 29, 2018

Public Version Number

2

DI Record Publish Date

June 06, 2016

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-