Catalog Number

-

Brand Name

cannulaCC

Version/Model Number

CC151520

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

August 10, 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

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

-

Product Code

GXI

Product Code Name

Probe, Radiofrequency Lesion

Public Device Record Key

c99f0ddf-f4be-417b-814d-531f3920d8ec

Public Version Date

June 10, 2022

Public Version Number

5

DI Record Publish Date

October 19, 2016

Package DI Number

08132500106646

Quantity per Package

10

Contains DI Package

08132500119516

Package Discontinue Date

August 10, 2020

Package Status

Not in Commercial Distribution

Package Type

-