Catalog Number

96SS

Brand Name

Autoimmune EIA

Version/Model Number

96SS

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)

-

Over the Counter (OTC)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

K001900

Product Code

LRM

Product Code Name

ANTI-DNA ANTIBODY (ENZYME-LABELED), ANTIGEN, CONTROL

Public Device Record Key

ad88089d-2bdf-4f45-b920-420f115ad094

Public Version Date

July 29, 2021

Public Version Number

5

DI Record Publish Date

September 12, 2016

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-