K-ASSAY® RF / ASO Liquid Control - For use as a consistent test sample of known - KAMIYA BIOMEDICAL COMPANY, LLC

Duns Number:197934250

Device Description: For use as a consistent test sample of known concentration for monitoring assay conditions For use as a consistent test sample of known concentration for monitoring assay conditions for the listed constituents.

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More Product Details

Catalog Number

K125C-2M

Brand Name

K-ASSAY® RF / ASO Liquid Control

Version/Model Number

K125C-2M

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

June 18, 2021

Issuing Agency

In GS1

Product Characteristics

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)

Yes

Over the Counter (OTC)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

-

Product Code Details

Product Code

JJX

Product Code Name

Single (Specified) Analyte Controls (Assayed And Unassayed)

Device Record Status

Public Device Record Key

f7630837-b4e2-4040-87e0-19577a808c1d

Public Version Date

June 21, 2021

Public Version Number

3

DI Record Publish Date

September 16, 2016

Additional Identifiers

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-

"KAMIYA BIOMEDICAL COMPANY, LLC" Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 49
2 A medical device with a moderate to high risk that requires special controls. 66