PMA
P800019: CYBERLITH IV UNIPOLAR PULSE GENERATOR
FDA PMA · Implantable pulse generator, pacemaker (non-CRT) · Boston Scientific
Key facts
| PMA number | P800019 |
|---|---|
| Trade name | CYBERLITH IV UNIPOLAR PULSE GENERATOR |
| Generic name | Implantable pulse generator, pacemaker (non-CRT) |
| Applicant | Boston Scientific |
| Owner/operator | Boston Scientific Corporation |
| Product code | LWP |
| Approval date | Mar 6, 1981 |
| Notice date | Jun 9, 1981 |
| Establishment registration | 2124215 |
| FEI number | 2124215 |
At a glance
- 10–99 Supplements
- Apr 23, 2012 Latest supplement decision
- Yes Withdrawn
- No Summary of safety and effectiveness on file
- None 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: