Catalog Number

-

Brand Name

Syringes (w/o needle)

Version/Model Number

6992

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)

-

Over the Counter (OTC)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

K060211,K060211,K060211

Product Code

FMF

Product Code Name

Syringe, Piston

Public Device Record Key

7c7e43f3-b108-4a01-b510-90215e6cae60

Public Version Date

July 06, 2018

Public Version Number

3

DI Record Publish Date

September 24, 2016

Package DI Number

00616784699233

Quantity per Package

10

Contains DI Package

00616784699226

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-