Duns Number:600593800
Catalog Number
-
Brand Name
Gallant™ PTCA Dilatation Catheter
Version/Model Number
SCG250R15US
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"
Yes
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
K173581
Product Code
LOX
Product Code Name
Catheters, Transluminal Coronary Angioplasty, Percutaneous
Public Device Record Key
054e6b31-69a4-4bbf-804a-097f7ba9ec13
Public Version Date
October 07, 2019
Public Version Number
2
DI Record Publish Date
August 15, 2018
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. | 83 |
3 | A medical device with high risk that requires premarket approval | 89 |