Catalog Number

-

Brand Name

CAPNOSTAT 5

Version/Model Number

6882078

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

K151814,K180098,K201874

Product Code

CBK

Product Code Name

Ventilator, Continuous, Facility Use

Public Device Record Key

fe3f5cbe-5c88-4491-88af-e69413be3443

Public Version Date

June 09, 2021

Public Version Number

5

DI Record Publish Date

January 27, 2016

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-