Catalog Number

-

Brand Name

Pipette

Version/Model Number

Pipette

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)

-

Over the Counter (OTC)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

K080278,K080278

Product Code

CCJ

Product Code Name

Analyzer, Gas, Carbon-Monoxide, Gaseous-Phase

Public Device Record Key

773557f0-4ebb-4405-90bd-fc069c605da5

Public Version Date

March 23, 2020

Public Version Number

4

DI Record Publish Date

September 15, 2017

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-