Catalog Number

930

Brand Name

Medegen Medical products

Version/Model Number

930

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In HIBCC

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)

-

Over the Counter (OTC)

-

Kit

-

Combination Product

-

Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)

-

FDA Premarket Submission

K942054,K942054

Product Code

FMI

Product Code Name

Needle, hypodermic, single lumen

Public Device Record Key

2a171873-8e72-4fdf-a993-7233bb4afeea

Public Version Date

July 06, 2018

Public Version Number

3

DI Record Publish Date

September 23, 2016

Package DI Number

H3629302

Quantity per Package

20

Contains DI Package

H3629300

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-