Catalog Number

AGD.A22

Brand Name

Dummy, silver, type CCY

Version/Model Number

AGD.A22

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

June 30, 2020

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

K931393

Product Code

KXK

Product Code Name

Source, Brachytherapy, Radionuclide

Public Device Record Key

a9f82a4e-6d23-4cbd-8aeb-98e2789d3c15

Public Version Date

July 01, 2020

Public Version Number

4

DI Record Publish Date

September 24, 2015

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-