Catalog Number

-

Brand Name

McKesson Cardiology

Version/Model Number

14.0

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)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

K112720

Product Code

LLZ

Product Code Name

System, Image Processing, Radiological

Public Device Record Key

421c7b6d-323a-4b96-9c6b-1be1aec360b8

Public Version Date

July 06, 2018

Public Version Number

3

DI Record Publish Date

March 09, 2017

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-