Catalog Number

73022

Brand Name

Kendall SCD

Version/Model Number

73022

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

-

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

-

Product Code

JOW

Product Code Name

SLEEVE, LIMB, COMPRESSIBLE

Public Device Record Key

f3eedab4-be25-4e91-8470-ca53cdf9593d

Public Version Date

August 11, 2020

Public Version Number

8

DI Record Publish Date

September 24, 2016

Package DI Number

40884521052087

Quantity per Package

5

Contains DI Package

30884521052080

Package Discontinue Date

January 26, 2005

Package Status

Not in Commercial Distribution

Package Type

CASE