Catalog Number

-

Brand Name

cannulaCC

Version/Model Number

CC5222

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

August 13, 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

24ff8452-0c69-4076-b0bc-7050170b8708

Public Version Date

June 10, 2022

Public Version Number

5

DI Record Publish Date

October 20, 2016

Package DI Number

08132500161164

Quantity per Package

10

Contains DI Package

08132500161096

Package Discontinue Date

August 13, 2020

Package Status

Not in Commercial Distribution

Package Type

-