Duns Number:020163218
Catalog Number
NR7TCS4Y
Brand Name
NaviStar RMT
Version/Model Number
NR7TCS4Y
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
P990025
Product Code
LPB
Product Code Name
Cardiac ablation percutaneous catheter
Public Device Record Key
10233a08-7609-4e7a-826f-067518aae22f
Public Version Date
June 07, 2022
Public Version Number
6
DI Record Publish Date
September 10, 2014
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. | 354 |
3 | A medical device with high risk that requires premarket approval | 183 |