Catalog Number

PD-2424

Brand Name

PREFERRED MEDICAL PRODUCTS, LLC

Version/Model Number

PD-2424

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)

Yes

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

K863853,K863853,K863853

Product Code

JAA

Product Code Name

System, X-Ray, Fluoroscopic, Image-Intensified

Public Device Record Key

86ec8d71-7369-4ef9-a066-d4a0463c3e99

Public Version Date

December 22, 2021

Public Version Number

3

DI Record Publish Date

May 20, 2019

Package DI Number

30680211002829

Quantity per Package

100

Contains DI Package

00680211002828

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

BOX