Catalog Number

-

Brand Name

Legionella IFA

Version/Model Number

IF0950

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

February 06, 2017

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

LHL

Product Code Name

Reagents, Antibody, Legionella, Direct & Indirect Fluorescent

Public Device Record Key

0f2602fd-5b24-44af-9348-5b172c219c80

Public Version Date

March 29, 2018

Public Version Number

2

DI Record Publish Date

September 22, 2016

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-