uTASWako AFP-L3 Control H - In-Vitro Diagnostic Use - FUJIFILM WAKO PURE CHEMICAL CORPORATION

Duns Number:690598875

Device Description: In-Vitro Diagnostic Use

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More Product Details

Catalog Number

993-61101

Brand Name

uTASWako AFP-L3 Control H

Version/Model Number

993-61101

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

October 23, 2020

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

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

K100464,K100464

Product Code Details

Product Code

JJX

Product Code Name

Single (Specified) Analyte Controls (Assayed And Unassayed)

Device Record Status

Public Device Record Key

2770a0c9-288b-412e-970c-db0e05efa32b

Public Version Date

October 26, 2020

Public Version Number

5

DI Record Publish Date

November 25, 2016

Additional Identifiers

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-

"FUJIFILM WAKO PURE CHEMICAL CORPORATION" Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 18
2 A medical device with a moderate to high risk that requires special controls. 22