Catalog Number

-

Brand Name

QUANTA Flash® aCL IgA Reagents

Version/Model Number

701225

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

Yes

Prescription Use (Rx)

Yes

Over the Counter (OTC)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

K120817

Product Code

MID

Product Code Name

System, Test, Anticardiolipin Immunological

Public Device Record Key

19f5756c-fba8-4574-80d6-eee8b430862d

Public Version Date

October 07, 2019

Public Version Number

1

DI Record Publish Date

September 27, 2019

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-