PMA supplement
P820014 S025: CORDIS SEQUICOR THETA MODELS 233D & 233E
FDA PMA supplement · Telectronics Pacing Systems, Inc.
Key facts
| Original PMA | P820014 |
|---|---|
| Supplement number | S025 |
| Trade name | CORDIS SEQUICOR THETA MODELS 233D & 233E |
| Generic name | Implantable pulse generator, pacemaker (non-CRT) |
| Applicant | Telectronics Pacing Systems, Inc. |
| Product code | LWP |
| Received date | Mar 26, 1986 |
| Decision date | May 5, 1986 |
At a glance
- No Expedited review granted
- No Approval order on file
- No Summary of safety and effectiveness on file
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About PMA supplements
A PMA supplement asks FDA to approve a change to a device that already holds a premarket approval: a new indication, a design or labeling change, a manufacturing site or process change.
Source: U.S. Food and Drug Administration (FDA), Premarket Approval (PMA) database · Source date: