Catalog Number

50300

Brand Name

QuickKart Procedure Cart

Version/Model Number

50300

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

K002764

Product Code

HRX

Product Code Name

Arthroscope

Public Device Record Key

848d5fda-97c1-4752-973d-90cfa32d47e4

Public Version Date

July 06, 2018

Public Version Number

3

DI Record Publish Date

August 21, 2017

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-