K-ASSAY® Apo AI/B Calibrator - For the calibration of the K-ASSAY® Apo AI and - KAMIYA BIOMEDICAL COMPANY, LLC

Duns Number:197934250

Device Description: For the calibration of the K-ASSAY® Apo AI and Apo B assays.

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More Product Details

Catalog Number

KAI-008C

Brand Name

K-ASSAY® Apo AI/B Calibrator

Version/Model Number

KAI-008C

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

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

K993606

Product Code Details

Product Code

JIX

Product Code Name

Calibrator, Multi-Analyte Mixture

Device Record Status

Public Device Record Key

8b6b9b9c-9163-4477-b09c-9dffb94eedab

Public Version Date

July 06, 2018

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