Catalog Number

-

Brand Name

Jelco

Version/Model Number

4317

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"

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

K014073,K014073,K014073

Product Code

FMF

Product Code Name

Syringe, piston

Public Device Record Key

0ee4e06f-f315-4214-9ffd-d3c4e27edfec

Public Version Date

July 06, 2018

Public Version Number

3

DI Record Publish Date

January 17, 2017

Package DI Number

30351688052036

Quantity per Package

8

Contains DI Package

10351688052032

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Case