Catalog Number

FH1650

Brand Name

DISPETTE®

Version/Model Number

FH1650

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

June 30, 2021

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)

Yes

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

-

Product Code

JPH

Product Code Name

Test, Erythrocyte Sedimentation Rate

Public Device Record Key

c038d0ba-a0da-4939-8c6a-e75f32d47d22

Public Version Date

October 20, 2021

Public Version Number

2

DI Record Publish Date

November 07, 2019

Package DI Number

07612964000809

Quantity per Package

10

Contains DI Package

07612964000762

Package Discontinue Date

June 30, 2021

Package Status

Not in Commercial Distribution

Package Type

CASE