Catalog Number

-

Brand Name

AnchorMarker

Version/Model Number

AM0845SL3-3

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

Yes

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

K083274

Product Code

KXK

Product Code Name

Source, Brachytherapy, Radionuclide

Public Device Record Key

b85cbb1a-1bac-42ab-adbe-a6aaccbbfa03

Public Version Date

June 10, 2022

Public Version Number

4

DI Record Publish Date

February 02, 2016

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-