Catalog Number

-

Brand Name

Single Use Aspiration Needle

Version/Model Number

NA-201SX-4021

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

August 10, 2022

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

-

Product Code

FCG

Product Code Name

Biopsy needle

Public Device Record Key

dffbc14e-00eb-431e-96f8-99f4ce11e78e

Public Version Date

August 11, 2022

Public Version Number

3

DI Record Publish Date

July 02, 2018

Package DI Number

14953170381918

Quantity per Package

5

Contains DI Package

04953170381911

Package Discontinue Date

August 10, 2022

Package Status

Not in Commercial Distribution

Package Type

-