Catalog Number

612083

Brand Name

TYSHAK NuCLEUS™

Version/Model Number

612083

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"

Yes

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

K121859

Product Code

DQY

Product Code Name

CATHETER, PERCUTANEOUS

Public Device Record Key

9ba6d974-e002-4dfe-a0d0-872af0ee346c

Public Version Date

March 25, 2020

Public Version Number

5

DI Record Publish Date

August 09, 2016

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-