Catalog Number

-

Brand Name

EMMA™ Capnometer Kit

Version/Model Number

kPa

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

February 16, 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

-

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

-

Product Code Name

-

Public Device Record Key

ff0c7694-60fc-4b3c-a09d-3efcb6e71d49

Public Version Date

February 17, 2021

Public Version Number

7

DI Record Publish Date

August 11, 2016

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-