Catalog Number

FGWG-500

Brand Name

LifeGlobal® Media

Version/Model Number

FGWG-500

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

July 06, 2019

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

K023033

Product Code

MQL

Product Code Name

MEDIA, REPRODUCTIVE

Public Device Record Key

c3aa73b5-fa0d-496d-ad21-f571a8de8398

Public Version Date

July 01, 2020

Public Version Number

4

DI Record Publish Date

September 21, 2016

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-