| Device |
temporary catheter, embolic protection, transcatheter intracardiac procedures |
| Regulation Description |
Temporary catheter for embolic protection during transcatheter intracardiac procedures. |
| Definition |
Embolic protection for transcatheter intracardiac procedures |
| Physical State |
This device is a single use percutaneous catheter system that has (a) blood filter(s) at the distal end and is introduced into an artery through the skin using a guidewire. |
| Technical Method |
This device is a single use percutaneous catheter system that is introduced into an artery. |
| Target Area |
Aortic arch or aortic arch branch vessels. |
| Regulation Medical Specialty |
Cardiovascular |
| Review Panel |
Cardiovascular |
| Product Code | PUM |
| Premarket Review |
Circulatory Support, Structural and Vascular Devices
(DHT2B)
Circulatory Support, Structural and Vascular Devices
(DHT2B)
|
| Submission Type |
510(k)
|
| Regulation Number |
870.1251
|
| Device Class |
2
|
| Total Product Life Cycle (TPLC) |
TPLC Product Code Report
|
| GMP Exempt? |
No
|
Summary Malfunction Reporting |
Ineligible |
| Implanted Device? |
No
|
| Life-Sustain/Support Device? |
No
|
| Third Party Review |
Not Third Party Eligible |