Catalog Number

PS1251K

Brand Name

Bard® BrachySource® I-125 Implant Seed

Version/Model Number

PS1251K

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

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

K093663

Product Code

KXK

Product Code Name

Source, brachytherapy, radionuclide

Public Device Record Key

84cd6bca-3e85-484f-9a01-82fcdd0dac9b

Public Version Date

November 02, 2020

Public Version Number

3

DI Record Publish Date

September 29, 2015

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-