Duns Number:006261481
Device Description: GENERATOR 6800001AMR CARDIOBLATE EN
Catalog Number
-
Brand Name
Cardioblate®
Version/Model Number
6800001AMR
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)
-
Over the Counter (OTC)
-
Kit
-
Combination Product
-
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)
-
FDA Premarket Submission
K080509
Product Code
OCL
Product Code Name
Surgical Device, For cutting, coagulation, and/or ablation of tissue, including cardiac tissue
Public Device Record Key
2b339df4-a879-4e38-98c8-8e68e8ae96c4
Public Version Date
June 10, 2022
Public Version Number
5
DI Record Publish Date
June 16, 2016
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 |
|---|---|---|
| 1 | A medical device with low to moderate risk that requires general controls | 102 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 20495 |
| 3 | A medical device with high risk that requires premarket approval | 3601 |