PMA supplement
P920032 S005: MICRO-PACE DUAL-CHAMBER, DDD, TEMPORARY CARDIAC PACEMAKER
FDA PMA supplement · Normal 180 Day Track · Pace Medical
Key facts
| Original PMA | P920032 |
|---|---|
| Supplement number | S005 |
| Supplement type | Normal 180 Day Track |
| Reason for the supplement | Location Change - Manufacturer/Sterilizer/Packager/Supplier |
| Trade name | MICRO-PACE DUAL-CHAMBER, DDD, TEMPORARY CARDIAC PACEMAKER |
| Generic name | Generator, pulse, pacemaker, external programmable (for electrophysiological studies only) |
| Applicant | Pace Medical |
| Product code | JOQ |
| Received date | Jun 25, 1999 |
| Decision date | Feb 2, 2000 |
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: