| Device |
pacemaker, cardiac, external transcutaneous (non-invasive) |
| Regulation Description |
External transcutaneous cardiac pacemaker (noninvasive). |
| Regulation Medical Specialty |
Cardiovascular |
| Review Panel |
Cardiovascular |
| Product Code | DRO |
| Premarket Review |
Office of Cardiovascular Devices
(OHT2)
Cardiac Electrophysiology, Diagnostics, and Monitoring Devices
(DHT2A)
|
| Submission Type |
510(k)
|
| Regulation Number |
870.5550
|
| Device Class |
2
|
| Total Product Life Cycle (TPLC) |
TPLC Product Code Report
|
| GMP Exempt? |
No
|
Summary Malfunction Reporting |
Eligible |
| Implanted Device? |
No
|
| Life-Sustain/Support Device? |
Yes
|
| Third Party Review |
Not Third Party Eligible |
|
|