Catalog Number

-

Brand Name

GenASIs™ System

Version/Model Number

GenASIs

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

January 25, 2018

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)

-

Over the Counter (OTC)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

K050236,K071398,K101291,K140957,K012103,K110345,K122554

Product Code

JOY

Product Code Name

Device, Automated Cell-Locating

Public Device Record Key

a73e2a2b-ee70-44a1-b751-e59e7e8059af

Public Version Date

March 22, 2022

Public Version Number

4

DI Record Publish Date

January 12, 2017

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-