Duns Number:305302119
Catalog Number
C-CAE-14.0-70-FII
Brand Name
COOK
Version/Model Number
G23646
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)
Yes
Over the Counter (OTC)
-
Kit
-
Combination Product
-
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)
-
FDA Premarket Submission
K161813
Product Code
BTR
Product Code Name
Tube, tracheal (w/wo connector)
Public Device Record Key
4fd71df1-103a-43bd-9a2b-420e90fa8e95
Public Version Date
February 18, 2019
Public Version Number
1
DI Record Publish Date
January 18, 2019
Package DI Number
None
Quantity per Package
-
Contains DI Package
-
Package Discontinue Date
-
Package Status
-
Package Type
-
Device Class | Device Class Description | No of Devices |
---|---|---|
2 | A medical device with a moderate to high risk that requires special controls. | 64 |
3 | A medical device with high risk that requires premarket approval | 273 |