Catalog Number

8-004-0017

Brand Name

Multicare Platinum

Version/Model Number

8-004-0017

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

K030666

Product Code

IZH

Product Code Name

System, x-ray, mammographic

Public Device Record Key

86f345a3-32f6-4d9f-b01b-dc211000224d

Public Version Date

July 06, 2018

Public Version Number

3

DI Record Publish Date

March 30, 2017

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-