Catalog Number

-

Brand Name

Advantage I-125®

Version/Model Number

RSLN-07

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In HIBCC

MRI safety Status

MR Conditional

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

K141701,K141701

Product Code

KXK

Product Code Name

Source, Brachytherapy, Radionuclide

Public Device Record Key

e7149082-8ce4-4a7b-bcaa-65299a5668b3

Public Version Date

July 06, 2018

Public Version Number

3

DI Record Publish Date

February 11, 2016

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-