PMA
P840068: DELTA PACEMAKER SYS; VIGOR DDD MODEL 950
FDA PMA · Implantable pulse generator, pacemaker (non-CRT) · Boston Scientific
Key facts
| PMA number | P840068 |
|---|---|
| Trade name | DELTA PACEMAKER SYS; VIGOR DDD MODEL 950 |
| Generic name | Implantable pulse generator, pacemaker (non-CRT) |
| Applicant | Boston Scientific |
| Owner/operator | Boston Scientific Corporation |
| Product code | LWP |
| Approval date | Nov 27, 1985 |
| Docket number | 85M-0579 |
| Notice date | Jan 24, 1986 |
| Establishment registration | 2124215 |
| FEI number | 2124215 |
At a glance
- 10–99 Supplements
- Apr 2, 2021 Latest supplement decision
- No Withdrawn
- No 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: