Catalog Number

-

Brand Name

Syringe, 3cc

Version/Model Number

0295-005-000

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)

Yes

Over the Counter (OTC)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

K844214,K844214

Product Code

LXC

Product Code Name

Monitor, Pressure, Intracompartmental

Public Device Record Key

9cea9f38-7e88-4625-9059-0a95502caaa8

Public Version Date

May 10, 2021

Public Version Number

2

DI Record Publish Date

April 08, 2020

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-