Catalog Number

591

Brand Name

Chrono-log

Version/Model Number

591

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

K962426

Product Code

JOZ

Product Code Name

System, Automated Platelet Aggregation

Public Device Record Key

730a41a0-4b0e-4f21-b808-605c2b02d130

Public Version Date

September 16, 2022

Public Version Number

4

DI Record Publish Date

October 11, 2016

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-