Catalog Number

VI410-1200

Brand Name

Synermed®

Version/Model Number

VI410-1200

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

-

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

K931958

Product Code

JQB

Product Code Name

Kinetic Method, Gamma-Glutamyl Transpeptidase

Public Device Record Key

0aa9c39b-e19a-4756-b3dd-a5a91cb8c37f

Public Version Date

July 06, 2018

Public Version Number

3

DI Record Publish Date

February 28, 2017

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-