Catalog Number

-

Brand Name

Blackford Platform

Version/Model Number

2.3.x

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)

-

Over the Counter (OTC)

Yes

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

K142337

Product Code

LLZ

Product Code Name

System, Image Processing, Radiological

Public Device Record Key

22639f90-8e23-48c2-8add-b4b89e658319

Public Version Date

April 22, 2021

Public Version Number

1

DI Record Publish Date

April 14, 2021

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-