Catalog Number

-

Brand Name

ArjoHuntleigh DVT Sleeve

Version/Model Number

RM-FG200

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)

Yes

Over the Counter (OTC)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

K031559,K031559

Product Code

JOW

Product Code Name

Sleeve, Limb, Compressible

Public Device Record Key

6c730d9c-9b97-4284-ae8a-25c45244b7a2

Public Version Date

August 02, 2019

Public Version Number

4

DI Record Publish Date

August 23, 2016

Package DI Number

10816317020245

Quantity per Package

10

Contains DI Package

00816317020248

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

CASE