PMA
P960016: LIVEWIRE(R) CARDIAC ABLATION SYSTEM
FDA PMA · Cardiac ablation percutaneous catheter · St Jude Medical
Key facts
| PMA number | P960016 |
|---|---|
| Trade name | LIVEWIRE(R) CARDIAC ABLATION SYSTEM |
| Generic name | Cardiac ablation percutaneous catheter |
| Applicant | St Jude Medical |
| Owner/operator | ABBOTT LABORATORIES |
| Product code | LPB |
| Approval date | May 4, 1999 |
| Docket number | 99M-1851 |
| Notice date | Jun 24, 1999 |
| Establishment registration | 3012179728 |
| FEI number | 1000526851 |
At a glance
- 10–99 Supplements
- Aug 7, 2026 Latest supplement decision
- No Withdrawn
- Yes Summary of safety and effectiveness on file
- 10–99 UDI device identifiers (GUDID)
- None MAUDE adverse event reports
- None Recall events
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About PMA approvals
Premarket approval (PMA) is the FDA's most stringent review pathway, required for most Class III devices that support or sustain life or present a potentially unreasonable risk.
Source: U.S. Food and Drug Administration (FDA), Premarket Approval (PMA) database · Source date: