Catalog Number

-

Brand Name

LC-40D XR CL

Version/Model Number

228-65000-55

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

KIE

Product Code Name

Apparatus, High Pressure Liquid Chromatography

Public Device Record Key

43db8108-07d6-4b15-b899-ae34cb8be6b0

Public Version Date

September 16, 2022

Public Version Number

2

DI Record Publish Date

January 15, 2021

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-