Catalog Number

FG3019

Brand Name

Access Needle

Version/Model Number

FG3019

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"

-

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

K113742

Product Code

HRX

Product Code Name

Arthroscope

Public Device Record Key

55dd510b-8e16-4b32-850a-a8507afabb8c

Public Version Date

June 08, 2020

Public Version Number

1

DI Record Publish Date

May 31, 2020

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-